---
OA_place: publisher
OA_type: gold
_id: '18515'
abstract:
- lang: eng
  text: "Understanding the role of evolutionary processes in shaping genetic variation
    has been a\r\nprimary goal in evolutionary genetics. In this regard, a key question
    is how genetically\r\ndistinct populations evolve in the face of gene flow, thereby
    generating genetic and\r\nphenotypic divergence and reproductive isolation (RI).
    This requires quantifying the role\r\nand relative contributions of prezygotic
    and postzygotic isolating mechanisms on the\r\nreduction of gene exchange between
    populations, and identifying regions in the genome\r\nthat mediate RI, which is
    often polygenic. Further, this needs distinguishing neutral and\r\nselected regions
    in the genome, and discerning how selection influences patterns of neutral\r\ndivergence.\r\nPopulation
    structure, defined as any deviation from panmixia, such as geographic distribution,
    movement and mating patterns of individuals, influences how genetic variation
    is\r\nstructured in space and shapes the neutral null model. Availability of large
    scale spatial\r\ngenomic datasets now enables us to detect signatures of population
    structure in genetic\r\ndata and infer population genetic parameters. Such inferences
    are crucial and have wide\r\napplications in biodiversity, conservation genetics,
    population management and medical\r\ngenetics. However, inferences are based on
    assumptions that do not always match the\r\ncomplex reality, thus leading to erroneous
    conclusions. Moreover, the role and interaction\r\nof heterogeneous population
    density and dispersal, which are ubiquitous in nature, has\r\nbeen challenging
    to study owing to their mathematical complexity. In such scenarios,\r\nfeedback
    between theory, data and simulations can prove to be useful.\r\nIn this thesis,
    I examine the effect of population structure on neutral genetic variation\r\nand
    barriers to gene exchange in hybridising populations, thereby bridging together
    the\r\nfields of spatial population genetics and speciation.\r\nDespite being
    a key concept in speciation, reproductive isolation (RI) lacks a quantitative\r\ndefinition
    and has been used and measured differently across different fields. Chapter 2\r\ngives
    a quantitative definition of RI, in terms of the effect of genetic differences
    on gene\r\nflow. We give analytical predictions for RI in a range of scenarios,
    in terms of effective migration rates for discrete populations and barrier strength
    for continuous populations.\r\nIn addition to this, we discuss current measures
    of RI and their limitations, and propose\r\nthe need for new measures that combine
    organismal and genetic perspectives of RI.\r\nIn chapter 3, I examine the combined
    effect of assortative mating, sexual selection\r\nand viability selection on RI.
    For this, we consider a polygenic ‘magic’ trait under a\r\nmainland-island model.
    We obtain novel theoretical predictions for molecular divergence\r\nin terms of
    effective migration rates, which bears a simple relationship to measurable\r\nfitness
    components of migrants and various early generation hybrids. We explore the\r\nconditions
    under which local adaptation can be maintained despite maladaptive gene flow\r\nand
    quantify the relative contributions of viability and sexual selection to genome-wide\r\nbarriers
    to gene flow.\r\nThe next two chapters of the thesis focus on a hybrid zone of
    Antirrhinum majus that\r\nconsist of two subspecies- the magenta flowered A. m.
    pseudomajus and the yellow\r\nflowered A.m. striatum. Previous studies have suggested
    that flower colour is target of\r\npollinator mediated selection and is influenced
    only by few genes. While these regions\r\nshow high genetic differentiation between
    the subspecies, the rest of the genome is seen\r\nto be well mixed. Chapter 4
    examines the effects of heterogeneous population density\r\nand leptokurtic dispersal
    on isolation by distance and the distribution of heterozygosity\r\nby focusing
    on non-flower colour markers.\r\nChapter 5 analyses cline shapes and associations
    among 6 focal flower colour markers to\r\nunderstand how selection and dispersal
    maintain this hybrid zone. We see sharp coincident\r\nstepped clines at all loci
    and positive associations throughout the hybrid zone, contrary to\r\nthe expected
    patterns from diffusive gene flow. With a novel scheme of inferring dispersal\r\ncombined
    with multilocus simulations, we show that stepped clines do not reflect genetic\r\nbarriers
    to gene flow, but are rather a result of long-distance migration. This framework\r\nallows
    us to get realistic estimates gene flow and selection and shows how traditional
    cline\r\nanalysis may lead to inaccurate conclusions when assumptions of the theory
    are not met.\r\nOverall, this thesis investigates how different features of population
    structure leave\r\ndetectable signatures in genetic variation, namely in patterns
    of isolation by distance,\r\nlinkage disequilibrium and genetic divergence. It
    also highlights how effective migration\r\nrates provide useful way of analysing
    polygenic architectures and shed new light into\r\nhybrid zones. In doing so,
    I identify scenarios when simple models become insufficient\r\nand suggest possibe
    directions by combining genetic data with simulations."
acknowledged_ssus:
- _id: ScienComp
acknowledgement: "I also acknowledge the funding agencies Marie Curie COFUND Doctoral
  Fellowship,\r\nAustrian Science Fund FWF (grant P32166) and ERC (grant PR1000ERC02)
  for financially\r\nsupporting my research over the years."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Parvathy
  full_name: Surendranadh, Parvathy
  id: 455235B8-F248-11E8-B48F-1D18A9856A87
  last_name: Surendranadh
  orcid: 0000-0001-6395-386X
citation:
  ama: Surendranadh P. Effect of population structure on neutral genetic variation
    and barriers to gene exchange. 2024. doi:<a href="https://doi.org/10.15479/at:ista:18515">10.15479/at:ista:18515</a>
  apa: Surendranadh, P. (2024). <i>Effect of population structure on neutral genetic
    variation and barriers to gene exchange</i>. Institute of Science and Technology
    Austria. <a href="https://doi.org/10.15479/at:ista:18515">https://doi.org/10.15479/at:ista:18515</a>
  chicago: Surendranadh, Parvathy. “Effect of Population Structure on Neutral Genetic
    Variation and Barriers to Gene Exchange.” Institute of Science and Technology
    Austria, 2024. <a href="https://doi.org/10.15479/at:ista:18515">https://doi.org/10.15479/at:ista:18515</a>.
  ieee: P. Surendranadh, “Effect of population structure on neutral genetic variation
    and barriers to gene exchange,” Institute of Science and Technology Austria, 2024.
  ista: Surendranadh P. 2024. Effect of population structure on neutral genetic variation
    and barriers to gene exchange. Institute of Science and Technology Austria.
  mla: Surendranadh, Parvathy. <i>Effect of Population Structure on Neutral Genetic
    Variation and Barriers to Gene Exchange</i>. Institute of Science and Technology
    Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:18515">10.15479/at:ista:18515</a>.
  short: P. Surendranadh, Effect of Population Structure on Neutral Genetic Variation
    and Barriers to Gene Exchange, Institute of Science and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-11-06T21:25:37Z
date_published: 2024-11-07T00:00:00Z
date_updated: 2026-04-07T12:56:52Z
day: '07'
ddc:
- '576'
degree_awarded: PhD
department:
- _id: GradSch
- _id: NiBa
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language:
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month: '11'
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oa_version: Published Version
page: '219'
project:
- _id: 05959E1C-7A3F-11EA-A408-12923DDC885E
  grant_number: P32166
  name: Snapdragon Speciation
- _id: bd6958e0-d553-11ed-ba76-86eba6a76c00
  grant_number: '101055327'
  name: Understanding the evolution of continuous genomes
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
title: Effect of population structure on neutral genetic variation and barriers to
  gene exchange
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  short: CC BY-NC-SA (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '18568'
abstract:
- lang: eng
  text: "Locomotion is ubiquitous in the animal kingdom because an animal's survival
    depends on its ability to navigate its environment to find food, avoid predators
    and locate potential mates. These behaviours require control mechanisms that can
    extract information from the environment, particularly visual cues. Selective
    evolutionary pressures have thus refined such visuomotor transformations in a
    species-specific manner to meet the specific ecological and ethological challenges
    of each organism. However, a common challenge across organisms as visual information
    processing\r\nbecomes increasingly detailed is the mechanisms required to synthesise
    disparate pieces of information into a coherent percept or unified picture of
    the world. In this thesis, I investigate how disparate visual information is combined
    in the brain of Drosophila melanogaster to effectively guide locomotion.\r\nFor
    this, I first designed and built a behavioural setup to record locomotion and
    present visual stimuli to freely-walking fruit flies in a closed-loop manner.
    This setup allowed the investigation of innate visually-guided behaviours, including
    the optomotor reflex and courtship.\r\nSecond, taking advantage of my system I
    investigated the optomotor response, a reflexive visual stabilisation behaviour
    in which flies turn in the direction of global motion to minimise retinal slip.
    This behaviour is thought to be mediated by Lobula plate tangential cells (LPTCs);
    a complex network of optic-flow-sensitive neurons essential for self-motion estimation.
    Using a novel genetic mutant, I demonstrate that electrical coupling between two
    LPTC subtypes, contralateral HS and H2 neurons, regulates the balance between
    smooth optomotor turning and saccadic anti-optomotor responses. These findings
    underscore the critical role of binocular motion cue integration in guiding course
    control. Finally, I developed a novel behavioural paradigm in which a sexually
    aroused male fruit fly is presented with an optomotor distractor. This setup creates
    competition between two visual behaviours, courtship tracking and the  optomotor
    response, enabling me to explore how the visual system resolves this conflict.
    In this setting, males\r\nengaged in courtship selectively suppress their optomotor
    response based on the female's location. Furthermore, when this experiment is
    replicated with an “artificial female”, optogenetically aroused males alternate
    between tracking and optomotor responses. The probability and dynamics of this
    switching are determined by the relative strengths of the two competing stimuli.
    In summary, the results presented in this thesis explore two mechanisms – integration
    and competition - through which visual information is combined in the brain of
    the fruit fly to drive locomotion."
acknowledged_ssus:
- _id: M-Shop
acknowledgement: I am incredibly thankful for the outstanding support provided by
  ISTA, especially the Machine Shop team, who made conducting research much easier
  and more efficient. I am also grateful for the funding provided by European Union’s
  Horizon 2020 research and innovation program under the Marie Skłodowska-Curie programme
  (665385) and The German Research Foundation grant DFG (SPP2205) “Evolutionary optimization
  of neuronal processing”.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Roshan K
  full_name: Satapathy, Roshan K
  id: 46046B7A-F248-11E8-B48F-1D18A9856A87
  last_name: Satapathy
  orcid: 0009-0006-2974-5075
citation:
  ama: Satapathy RK. Mechanisms of visual integration and competition in innate behaviours
    in Drosophila melanogaster. 2024. doi:<a href="https://doi.org/10.15479/at:ista:18568">10.15479/at:ista:18568</a>
  apa: Satapathy, R. K. (2024). <i>Mechanisms of visual integration and competition
    in innate behaviours in Drosophila melanogaster</i>. Institute of Science and
    Technology Austria. <a href="https://doi.org/10.15479/at:ista:18568">https://doi.org/10.15479/at:ista:18568</a>
  chicago: Satapathy, Roshan K. “Mechanisms of Visual Integration and Competition
    in Innate Behaviours in Drosophila Melanogaster.” Institute of Science and Technology
    Austria, 2024. <a href="https://doi.org/10.15479/at:ista:18568">https://doi.org/10.15479/at:ista:18568</a>.
  ieee: R. K. Satapathy, “Mechanisms of visual integration and competition in innate
    behaviours in Drosophila melanogaster,” Institute of Science and Technology Austria,
    2024.
  ista: Satapathy RK. 2024. Mechanisms of visual integration and competition in innate
    behaviours in Drosophila melanogaster. Institute of Science and Technology Austria.
  mla: Satapathy, Roshan K. <i>Mechanisms of Visual Integration and Competition in
    Innate Behaviours in Drosophila Melanogaster</i>. Institute of Science and Technology
    Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:18568">10.15479/at:ista:18568</a>.
  short: R.K. Satapathy, Mechanisms of Visual Integration and Competition in Innate
    Behaviours in Drosophila Melanogaster, Institute of Science and Technology Austria,
    2024.
corr_author: '1'
date_created: 2024-11-19T12:34:30Z
date_published: 2024-11-20T00:00:00Z
date_updated: 2026-04-07T13:00:36Z
day: '20'
ddc:
- '573'
degree_awarded: PhD
department:
- _id: GradSch
- _id: MaJö
doi: 10.15479/at:ista:18568
ec_funded: 1
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language:
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license: https://creativecommons.org/licenses/by-sa/4.0/
month: '11'
oa: 1
oa_version: Published Version
page: '114'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  isbn:
  - 978-3-99078-047-3
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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  - id: '18444'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Maximilian A
  full_name: Jösch, Maximilian A
  id: 2BD278E6-F248-11E8-B48F-1D18A9856A87
  last_name: Jösch
  orcid: 0000-0002-3937-1330
title: Mechanisms of visual integration and competition in innate behaviours in Drosophila
  melanogaster
tmp:
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    BY-SA 4.0)
  short: CC BY-SA (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '18674'
abstract:
- lang: eng
  text: Mapping the complex and dense arrangement of cells and their connectivity
    in brain tissue requires volumetric imaging at nanoscale spatial resolution. While
    light microscopy excels at visualizing specific molecules and individual cells,
    achieving dense, synapse-level circuit reconstruction has not been possible with
    any light microscopy technique. Thus, the goal of my work was to develop image
    and data analysis pipelines for brain tissue visualization and reconstruction
    with light microscopy. To achieve dense circuit reconstruction with single-synapse
    resolution, I developed both conventional and deep-learning-based synapse detection
    algorithms, as well as connectivity analysis pipelines that integrate synapse
    detection with volumetric segmentation of brain tissue.
acknowledged_ssus:
- _id: Bio
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Julia
  full_name: Lyudchik, Julia
  id: 46E28B80-F248-11E8-B48F-1D18A9856A87
  last_name: Lyudchik
citation:
  ama: Lyudchik J. Image analysis for brain tissue reconstruction with super-resolution
    light microscopy. 2024. doi:<a href="https://doi.org/10.15479/at:ista:18674">10.15479/at:ista:18674</a>
  apa: Lyudchik, J. (2024). <i>Image analysis for brain tissue reconstruction with
    super-resolution light microscopy</i>. Institute of Science and Technology Austria.
    <a href="https://doi.org/10.15479/at:ista:18674">https://doi.org/10.15479/at:ista:18674</a>
  chicago: Lyudchik, Julia. “Image Analysis for Brain Tissue Reconstruction with Super-Resolution
    Light Microscopy.” Institute of Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:18674">https://doi.org/10.15479/at:ista:18674</a>.
  ieee: J. Lyudchik, “Image analysis for brain tissue reconstruction with super-resolution
    light microscopy,” Institute of Science and Technology Austria, 2024.
  ista: Lyudchik J. 2024. Image analysis for brain tissue reconstruction with super-resolution
    light microscopy. Institute of Science and Technology Austria.
  mla: Lyudchik, Julia. <i>Image Analysis for Brain Tissue Reconstruction with Super-Resolution
    Light Microscopy</i>. Institute of Science and Technology Austria, 2024, doi:<a
    href="https://doi.org/10.15479/at:ista:18674">10.15479/at:ista:18674</a>.
  short: J. Lyudchik, Image Analysis for Brain Tissue Reconstruction with Super-Resolution
    Light Microscopy, Institute of Science and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-12-18T14:24:43Z
date_published: 2024-12-18T00:00:00Z
date_updated: 2026-04-14T08:34:35Z
day: '18'
ddc:
- '004'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JoDa
doi: 10.15479/at:ista:18674
ec_funded: 1
file:
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month: '12'
oa: 1
oa_version: Published Version
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  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  isbn:
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  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
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    relation: part_of_dissertation
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  - id: '14257'
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    status: public
status: public
supervisor:
- first_name: Johann G
  full_name: Danzl, Johann G
  id: 42EFD3B6-F248-11E8-B48F-1D18A9856A87
  last_name: Danzl
  orcid: 0000-0001-8559-3973
title: Image analysis for brain tissue reconstruction with super-resolution light
  microscopy
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  short: CC BY-NC-ND (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_embargo: '20'
OA_place: publisher
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acknowledged_ssus:
- _id: Bio
- _id: PreCl
- _id: LifeSc
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Mojtaba
  full_name: Tavakoli, Mojtaba
  id: 3A0A06F4-F248-11E8-B48F-1D18A9856A87
  last_name: Tavakoli
  orcid: 0000-0002-7667-6854
citation:
  ama: 'Tavakoli M. Developing molecular and structural tools for studying brain architecture
    with super resolution expansion microscopy. LICONN: Molecularly-informed connectomics
    reconstruction with light microscopy. 2024. doi:<a href="https://doi.org/10.15479/at:ista:18681">10.15479/at:ista:18681</a>'
  apa: 'Tavakoli, M. (2024). <i>Developing molecular and structural tools for studying
    brain architecture with super resolution expansion microscopy. LICONN: Molecularly-informed
    connectomics reconstruction with light microscopy</i>. Institute of Science and
    Technology Austria. <a href="https://doi.org/10.15479/at:ista:18681">https://doi.org/10.15479/at:ista:18681</a>'
  chicago: 'Tavakoli, Mojtaba. “Developing Molecular and Structural Tools for Studying
    Brain Architecture with Super Resolution Expansion Microscopy. LICONN: Molecularly-Informed
    Connectomics Reconstruction with Light Microscopy.” Institute of Science and Technology
    Austria, 2024. <a href="https://doi.org/10.15479/at:ista:18681">https://doi.org/10.15479/at:ista:18681</a>.'
  ieee: 'M. Tavakoli, “Developing molecular and structural tools for studying brain
    architecture with super resolution expansion microscopy. LICONN: Molecularly-informed
    connectomics reconstruction with light microscopy,” Institute of Science and Technology
    Austria, 2024.'
  ista: 'Tavakoli M. 2024. Developing molecular and structural tools for studying
    brain architecture with super resolution expansion microscopy. LICONN: Molecularly-informed
    connectomics reconstruction with light microscopy. Institute of Science and Technology
    Austria.'
  mla: 'Tavakoli, Mojtaba. <i>Developing Molecular and Structural Tools for Studying
    Brain Architecture with Super Resolution Expansion Microscopy. LICONN: Molecularly-Informed
    Connectomics Reconstruction with Light Microscopy</i>. Institute of Science and
    Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:18681">10.15479/at:ista:18681</a>.'
  short: 'M. Tavakoli, Developing Molecular and Structural Tools for Studying Brain
    Architecture with Super Resolution Expansion Microscopy. LICONN: Molecularly-Informed
    Connectomics Reconstruction with Light Microscopy, Institute of Science and Technology
    Austria, 2024.'
corr_author: '1'
date_created: 2024-12-19T02:30:39Z
date_published: 2024-12-20T00:00:00Z
date_updated: 2026-04-07T12:56:37Z
day: '20'
ddc:
- '600'
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JoDa
doi: 10.15479/at:ista:18681
file:
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  checksum: b61651d417cafddd740a8528f46068c5
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  creator: mtavakol
  date_created: 2024-12-20T10:23:17Z
  date_updated: 2024-12-20T10:31:37Z
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language:
- iso: eng
month: '12'
oa_version: Published Version
page: '230'
project:
- _id: 6285a163-2b32-11ec-9570-8e204ca2dba5
  grant_number: '26137'
  name: Studying Organelle Structure and Function at Nanoscale Resolution with Expansion
    Microscopy
- _id: 26AA4EF2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W1232-B24
  name: Molecular Drug Targets
publication_identifier:
  isbn:
  - 978-3-99078-048-0
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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    relation: part_of_dissertation
    status: public
  - id: '18688'
    relation: part_of_dissertation
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  - id: '18677'
    relation: part_of_dissertation
    status: public
  - id: '18689'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Johann G
  full_name: Danzl, Johann G
  id: 42EFD3B6-F248-11E8-B48F-1D18A9856A87
  last_name: Danzl
  orcid: 0000-0001-8559-3973
title: 'Developing molecular and structural tools for studying brain architecture
  with super resolution expansion microscopy. LICONN: Molecularly-informed connectomics
  reconstruction with light microscopy'
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    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '18766'
abstract:
- lang: eng
  text: Poxviruses are large pleomorphic double-stranded DNA viruses that include
    well known members such as variola virus, the causative agent of smallpox, Mpox
    virus, as well as Vaccinia virus (VACV), which serves as a vaccination strain
    for formerly mentioned viruses. VACV is a valuable model for studying large pleomorphic
    DNA viruses in general and poxviruses specifically, as many features, such as
    core morphology and structural proteins, are well conserved within this family.
    Despite decades of research, our understanding of the structural components and
    proteins that comprise the poxvirus core in mature virions remains limited. Although
    major core proteins were identified via indirect experimental evidence, the core's
    complexity, with its large size, structure and number of involved proteins, has
    hindered efforts to achieve high-resolution insights and to define the roles of
    the individual proteins. The specific protein composition of the core's individual
    layers, including the palisade layer and the inner core wall, has remained unclear.
    In this study, we have merged multiple approaches, including single particle cryo
    electron microscopy of purified virus cores, cryo-electron tomography and subtomogram
    averaging of mature virions and molecular modeling to elucidate the structural
    determinants of the VACV core. Due to the lack of experimentally derived structures,
    either in situ or reconstituted in vitro, we used Alphafold to predict models
    of the putative major core protein candidates, A10, 23k, A3, A4, and L4. Our results
    show that the VACV core is composed of several layers with varying local symmetries,
    forming more intricate interactions than observed previously. This allowed us
    to identify several molecular building blocks forming the viral core lattice.
    In particular, we identified trimers of protein A10 as a major core structure
    that forms the palisade layer of the viral core. Additionally, we revealed that
    six petals of a flower shaped core pore within the core wall are composed of A10
    trimers. Furthermore, we obtained a cryo-EM density for the inner core wall that
    could potentially accommodate an A3 dimer. Integrating descriptions of protein
    interactions from previous studies enabled us to provide a detailed structural
    model of the poxvirus core wall, and our findings indicate that the interactions
    within A10 trimers are likely consistent across orthopox- and parapoxviruses.
    This combined application of cryo-SPA and cryo-ET can help overcome obstacles
    in studying complex virus structures in the future, including their key assembly
    proteins, interactions, and the formation into a core lattice. Our work provides
    important fundamental new insights into poxvirus core architecture, also considering
    the recent re-emergence of poxviruses.
acknowledged_ssus:
- _id: EM-Fac
- _id: LifeSc
- _id: ScienComp
acknowledgement: "This work was funded by the Austrian Science Fund (FWF) grant P31445
  and ISTA. I\r\nwould like to express my gratitude to the Scientific Service Units,
  particularly the Lab\r\nSupport Facility, the Scientific Computing Facility and
  the Electron Microscopy Facility\r\nfor their tremendous support. I want to especially
  thank Alois for assisting me with the\r\ninstallation of countless new software
  and for troubleshooting cluster issues. A special\r\nthanks goes to Valentin for
  his outstanding support in cryo-EM data acquisition and\r\nhis ongoing help in improving
  the process to ensure that I obtained the best possible\r\ndata from my sample."
alternative_title:
- ISTA thesis
article_processing_charge: No
author:
- first_name: Julia
  full_name: Datler, Julia
  id: 3B12E2E6-F248-11E8-B48F-1D18A9856A87
  last_name: Datler
  orcid: 0000-0002-3616-8580
citation:
  ama: Datler J. Elucidating the structural determinants of the poxvirus core using
    multi-modal cryo-EM. 2024. doi:<a href="https://doi.org/10.15479/at:ista:18766">10.15479/at:ista:18766</a>
  apa: Datler, J. (2024). <i>Elucidating the structural determinants of the poxvirus
    core using multi-modal cryo-EM</i>. Institute of Science and Technology Austria.
    <a href="https://doi.org/10.15479/at:ista:18766">https://doi.org/10.15479/at:ista:18766</a>
  chicago: Datler, Julia. “Elucidating the Structural Determinants of the Poxvirus
    Core Using Multi-Modal Cryo-EM.” Institute of Science and Technology Austria,
    2024. <a href="https://doi.org/10.15479/at:ista:18766">https://doi.org/10.15479/at:ista:18766</a>.
  ieee: J. Datler, “Elucidating the structural determinants of the poxvirus core using
    multi-modal cryo-EM,” Institute of Science and Technology Austria, 2024.
  ista: Datler J. 2024. Elucidating the structural determinants of the poxvirus core
    using multi-modal cryo-EM. Institute of Science and Technology Austria.
  mla: Datler, Julia. <i>Elucidating the Structural Determinants of the Poxvirus Core
    Using Multi-Modal Cryo-EM</i>. Institute of Science and Technology Austria, 2024,
    doi:<a href="https://doi.org/10.15479/at:ista:18766">10.15479/at:ista:18766</a>.
  short: J. Datler, Elucidating the Structural Determinants of the Poxvirus Core Using
    Multi-Modal Cryo-EM, Institute of Science and Technology Austria, 2024.
corr_author: '1'
date_created: 2025-01-07T10:23:12Z
date_published: 2024-12-30T00:00:00Z
date_updated: 2026-04-07T12:59:44Z
day: '30'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: FlSc
doi: 10.15479/at:ista:18766
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keyword:
- cryo-EM
- cryo-ET
- cryo-SPA
- Structural Virology
- Poxvirus
- Vaccinia Virus
- Structural Biology
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: '106'
project:
- _id: 26736D6A-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P31445
  name: Structural conservation and diversity in retroviral capsid
publication_identifier:
  isbn:
  - 978-3-99078-049-7
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
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    relation: part_of_dissertation
    status: public
  - id: '14979'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Florian KM
  full_name: Schur, Florian KM
  id: 48AD8942-F248-11E8-B48F-1D18A9856A87
  last_name: Schur
  orcid: 0000-0003-4790-8078
title: Elucidating the structural determinants of the poxvirus core using multi-modal
  cryo-EM
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  short: CC BY-NC-ND (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '17208'
abstract:
- lang: eng
  text: "Can current quantum computers provide a speedup over their classical counterparts
    for some kinds of problems? In this thesis, with a focus on ground state search/preparation,
    we address some of the challenges that both quantum annealing and variational
    quantum algorithms suffer from, hindering any possible practical speedup in comparison
    to the best classical counterparts. \r\n\r\nIn the first part of the thesis, we
    study the performance of quantum annealing for solving a particular combinatorial
    optimization problem called 3-XOR satisfability (3-XORSAT). The classical problem
    is mapped into a ground state search of a 3-local classical Hamiltonian $H_C$.
    We consider how modifying the initial problem, by adding more interaction terms
    to the corresponding Hamiltonian, leads to the emergence of a first-order phase
    transition during the annealing process. This phenomenon causes the total annealing
    duration, $T$, required to prepare the ground state of $H_C$ with a high probability
    to increase exponentially with the size of the problem. Our findings indicate
    that with the growing complexity of problem instances, the likelihood of encountering
    first-order phase transitions also increases, making quantum annealing an impractical
    solution for these types of combinatorial optimization problems.\r\n\r\nIn the
    second part, we focus on the problem of barren plateaus in generic variational
    quantum algorithms. Barren plateaus correspond to flat regions in the parameter
    space where the gradient of the cost function is zero in expectation, and with
    the variance decaying exponentially with the system size, thus obstructing an
    efficient parameter optimization.  We propose an algorithm to circumvent Barren
    Plateaus by monitoring the entanglement entropy of k-local reduced density matrices,
    alongside a method for estimating entanglement entropy via classical shadow tomography.
    We illustrate the approach with the paradigmatic example of the variational quantum
    eigensolver, and show that our algorithm effectively avoids barren plateaus in
    the initialization as well as during the optimization stage. \r\n\r\nLastly, in
    the last two Chapters of this thesis, we focus on the quantum approximate optimization
    algorithm (QAOA), originally introduced as an algorithm for solving generic combinatorial
    optimization problems in near-term quantum devices. Specifically, we focus on
    how to develop rigorous initialization strategies with guarantee improvement.
    Our motivation for this study lies in that for random initialization, the optimization
    typically leads to local minima with poor performance. Our main result corresponds
    to the analytical construction of index-1 saddle points or transition states,
    stationary points with a single direction of descent, as a tool for systematically
    exploring the QAOA optimization landscape. This leads us to propose a novel greedy
    parameter initialization strategy that guarantees for the energy to decrease with
    an increasing number of circuit layers. Furthermore, with precise estimates for
    the negative Hessian eigenvalue and its eigenvector, we establish a lower bound
    for energy improvement following a QAOA iteration."
acknowledged_ssus:
- _id: ScienComp
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Raimel A
  full_name: Medina Ramos, Raimel A
  id: CE680B90-D85A-11E9-B684-C920E6697425
  last_name: Medina Ramos
  orcid: 0000-0002-5383-2869
citation:
  ama: Medina Ramos RA. Exploring the optimization landscape of variational quantum
    algorithms. 2024. doi:<a href="https://doi.org/10.15479/at:ista:17208">10.15479/at:ista:17208</a>
  apa: Medina Ramos, R. A. (2024). <i>Exploring the optimization landscape of variational
    quantum algorithms</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:17208">https://doi.org/10.15479/at:ista:17208</a>
  chicago: Medina Ramos, Raimel A. “Exploring the Optimization Landscape of Variational
    Quantum Algorithms.” Institute of Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:17208">https://doi.org/10.15479/at:ista:17208</a>.
  ieee: R. A. Medina Ramos, “Exploring the optimization landscape of variational quantum
    algorithms,” Institute of Science and Technology Austria, 2024.
  ista: Medina Ramos RA. 2024. Exploring the optimization landscape of variational
    quantum algorithms. Institute of Science and Technology Austria.
  mla: Medina Ramos, Raimel A. <i>Exploring the Optimization Landscape of Variational
    Quantum Algorithms</i>. Institute of Science and Technology Austria, 2024, doi:<a
    href="https://doi.org/10.15479/at:ista:17208">10.15479/at:ista:17208</a>.
  short: R.A. Medina Ramos, Exploring the Optimization Landscape of Variational Quantum
    Algorithms, Institute of Science and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-07-09T09:14:24Z
date_published: 2024-07-09T00:00:00Z
date_updated: 2026-04-07T12:43:22Z
day: '09'
ddc:
- '539'
degree_awarded: PhD
department:
- _id: GradSch
- _id: MaSe
doi: 10.15479/at:ista:17208
ec_funded: 1
file:
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  date_updated: 2024-07-10T11:34:09Z
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  file_name: Raimel_Thesis-Final.zip
  file_size: '14218691'
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  checksum: 6724a95bec772dbabc0111b9f08a805e
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file_date_updated: 2024-07-17T09:23:24Z
has_accepted_license: '1'
keyword:
- Quantum computing
- Variational Quantum Algorithms
- Optimization
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '07'
oa: 1
oa_version: Published Version
page: '133'
project:
- _id: 23841C26-32DE-11EA-91FC-C7463DDC885E
  call_identifier: H2020
  grant_number: '850899'
  name: 'Non-Ergodic Quantum Matter: Universality, Dynamics and Control'
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '10545'
    relation: part_of_dissertation
    status: public
  - id: '10067'
    relation: part_of_dissertation
    status: public
  - id: '17222'
    relation: part_of_dissertation
    status: public
  - id: '13125'
    relation: part_of_dissertation
    status: public
  - id: '11471'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Maksym
  full_name: Serbyn, Maksym
  id: 47809E7E-F248-11E8-B48F-1D18A9856A87
  last_name: Serbyn
  orcid: 0000-0002-2399-5827
title: Exploring the optimization landscape of variational quantum algorithms
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  short: CC BY (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '17336'
abstract:
- lang: eng
  text: "This thesis deals with the study of stochastic processes and their ergodicity
    properties. The\r\nvariety of problems encountered calls for a set of different
    approaches, ranging from classical to\r\nmodern ones: a special place is held
    by probabilistic methods based on couplings, by functional\r\ninequalities, and
    by the theory of gradient flows in the space of measures.\r\n\r\nThe material
    is organized as follows. Chapter 1 contains the introduction to this thesis, starting\r\nwith
    a general presentation of some of the relevant topics. Section 1.1 is dedicated
    to the\r\ntheory of gradient flows in metric spaces, and introduces the first
    contribution of this thesis\r\n[DSMP24], which is presented in detail in Chapter
    2. Section 1.2 moves to the topic of\r\ncurvature of Markov chains, concluding
    with a brief description of our second contribution\r\n[Ped23], which is included
    in Chapter 3. Section 1.3 discusses applications of stochastic\r\nprocesses to
    the theory of sampling, in particular the recent framework of score-based diffusion\r\nmodels,
    and our contribution [PMM24], which is contained in Chapter 4. Section 1.4 discusses\r\nsome
    related problems, concerning the regularization properties of the heat flow. It
    serves\r\nas a motivation for the work [BP24], which we report in Chapter 5. Finally,
    Section 1.5\r\ndiscusses the last contribution of this thesis, which can be found
    in Chapter 6. It deals with\r\nthe convergence to equilibrium of a particular
    stochastic model from quantitative genetics:\r\nthis is established via some functional
    inequalities, which we prove with probabilistic arguments\r\nbased on couplings.\r\n"
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Francesco
  full_name: Pedrotti, Francesco
  id: d3ac8ac6-dc8d-11ea-abe3-e2a9628c4c3c
  last_name: Pedrotti
citation:
  ama: Pedrotti F. Functional inequalities and convergence of stochastic processes.
    2024. doi:<a href="https://doi.org/10.15479/at:ista:17336">10.15479/at:ista:17336</a>
  apa: Pedrotti, F. (2024). <i>Functional inequalities and convergence of stochastic
    processes</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:17336">https://doi.org/10.15479/at:ista:17336</a>
  chicago: Pedrotti, Francesco. “Functional Inequalities and Convergence of Stochastic
    Processes.” Institute of Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:17336">https://doi.org/10.15479/at:ista:17336</a>.
  ieee: F. Pedrotti, “Functional inequalities and convergence of stochastic processes,”
    Institute of Science and Technology Austria, 2024.
  ista: Pedrotti F. 2024. Functional inequalities and convergence of stochastic processes.
    Institute of Science and Technology Austria.
  mla: Pedrotti, Francesco. <i>Functional Inequalities and Convergence of Stochastic
    Processes</i>. Institute of Science and Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:17336">10.15479/at:ista:17336</a>.
  short: F. Pedrotti, Functional Inequalities and Convergence of Stochastic Processes,
    Institute of Science and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-07-29T09:14:14Z
date_published: 2024-07-31T00:00:00Z
date_updated: 2026-04-07T13:00:03Z
day: '31'
ddc:
- '500'
- '510'
- '515'
- '519'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JaMa
doi: 10.15479/at:ista:17336
ec_funded: 1
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has_accepted_license: '1'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: '183'
project:
- _id: 256E75B8-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '716117'
  name: Optimal Transport and Stochastic Dynamics
- _id: fc31cba2-9c52-11eb-aca3-ff467d239cd2
  grant_number: F6504
  name: Taming Complexity in Partial Differential Systems
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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    relation: part_of_dissertation
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  - id: '17350'
    relation: part_of_dissertation
    status: public
  - id: '17352'
    relation: part_of_dissertation
    status: public
  - id: '17143'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Jan
  full_name: Maas, Jan
  id: 4C5696CE-F248-11E8-B48F-1D18A9856A87
  last_name: Maas
  orcid: 0000-0002-0845-1338
title: Functional inequalities and convergence of stochastic processes
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  short: CC BY-NC-ND (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '17490'
abstract:
- lang: eng
  text: "Deep learning is essential in numerous applications nowadays, with many recent
    advancements made possible by training very large models. Despite their broad
    applicability, training neural networks is often time-intensive, and it is usually
    impractical to manage large models and datasets on a single machine. To address
    these issues, distributed deep learning training has become increasingly important.
    However, distributed training requires synchronization among nodes, and the mini-batch
    stochastic gradient descent algorithm places a significant load on network connections.
    A possible solution to tackle the synchronization bottleneck is to reduce a message
    size by lossy compression.\r\n\r\nIn this thesis, we investigate systems and algorithmic
    approaches to communication compression during training. From the systems perspective,
    we demonstrate that a common approach of expensive hardware overprovisioning can
    be replaced through a thorough system design. We introduce a framework that introduces
    efficient software support for compressed communication in machine learning applications,
    applicable to both multi-GPU single-node training and larger-scale multi-node
    training. Our framework integrates with popular ML frameworks, providing up to
    3x speedups for multi-GPU nodes based on commodity hardware and order-of-magnitude
    improvements in the multi-node setting, with negligible impact on accuracy.\r\n\r\nAlso,
    we consider an application of our framework to different communication schemes,
    such as Fully Sharded Data Parallel. We provide strong convergence guarantees
    for the compression in such a setup. Empirical validation shows that our method
    preserves model accuracy for GPT-family models with up to 1.3 billion parameters,
    while completely removing the communication bottlenecks of non-compressed alternatives,
    providing up to 2.2x speedups end-to-end.\r\n\r\nFrom the algorithmic side, we
    propose a general framework that dynamically adjusts the degree of compression
    across a model's layers during training. This approach enhances overall compression
    and results in significant speedups without compromising accuracy. Our algorithm
    utilizes an adaptive algorithm that automatically selects the optimal compression
    parameters for model layers, ensuring the best compression ratio while adhering
    to an error constraint. Our method is effective across all existing families of
    compression methods. It achieves up to 2.5x faster training and up to a 5x improvement
    in compression compared to efficient implementations of current approaches. Additionally,
    LGreCo can complement existing adaptive algorithms.\r\n"
acknowledged_ssus:
- _id: ScienComp
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Ilia
  full_name: Markov, Ilia
  id: D0CF4148-C985-11E9-8066-0BDEE5697425
  last_name: Markov
citation:
  ama: 'Markov I. Communication-efficient distributed training of deep neural networks :
    An algorithms and systems perspective. 2024. doi:<a href="https://doi.org/10.15479/at:ista:17490">10.15479/at:ista:17490</a>'
  apa: 'Markov, I. (2024). <i>Communication-efficient distributed training of deep
    neural networks : An algorithms and systems perspective</i>. Institute of Science
    and Technology Austria. <a href="https://doi.org/10.15479/at:ista:17490">https://doi.org/10.15479/at:ista:17490</a>'
  chicago: 'Markov, Ilia. “Communication-Efficient Distributed Training of Deep Neural
    Networks : An Algorithms and Systems Perspective.” Institute of Science and Technology
    Austria, 2024. <a href="https://doi.org/10.15479/at:ista:17490">https://doi.org/10.15479/at:ista:17490</a>.'
  ieee: 'I. Markov, “Communication-efficient distributed training of deep neural networks :
    An algorithms and systems perspective,” Institute of Science and Technology Austria,
    2024.'
  ista: 'Markov I. 2024. Communication-efficient distributed training of deep neural
    networks : An algorithms and systems perspective. Institute of Science and Technology
    Austria.'
  mla: 'Markov, Ilia. <i>Communication-Efficient Distributed Training of Deep Neural
    Networks : An Algorithms and Systems Perspective</i>. Institute of Science and
    Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:17490">10.15479/at:ista:17490</a>.'
  short: 'I. Markov, Communication-Efficient Distributed Training of Deep Neural Networks :
    An Algorithms and Systems Perspective, Institute of Science and Technology Austria,
    2024.'
corr_author: '1'
date_created: 2024-09-04T08:51:11Z
date_published: 2024-09-04T00:00:00Z
date_updated: 2026-06-18T17:55:23Z
day: '04'
ddc:
- '000'
degree_awarded: PhD
department:
- _id: GradSch
- _id: DaAl
doi: 10.15479/at:ista:17490
ec_funded: 1
file:
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  date_created: 2024-09-04T08:35:35Z
  date_updated: 2024-09-04T08:35:35Z
  file_id: '17491'
  file_name: Thesis.zip
  file_size: 43327753
  relation: source_file
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  content_type: application/pdf
  creator: imarkov
  date_created: 2024-09-04T08:36:06Z
  date_updated: 2024-09-04T08:36:06Z
  file_id: '17492'
  file_name: Thesis_final_version_pdfa2.pdf
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file_date_updated: 2024-09-04T08:36:06Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '102'
project:
- _id: 268A44D6-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '805223'
  name: Elastic Coordination for Scalable Machine Learning
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '14461'
    relation: part_of_dissertation
    status: public
  - id: '12780'
    relation: part_of_dissertation
    status: public
  - id: '17456'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
title: 'Communication-efficient distributed training of deep neural networks : An
  algorithms and systems perspective'
tmp:
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    BY-NC-SA 4.0)
  short: CC BY-NC-SA (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '17850'
abstract:
- lang: eng
  text: "Understanding the relationship between a given phenotype and its underlying
    genotype or genotypes is one of the most pressing challenges of biology, as it
    lies at the heart of not only basic understanding of evolutionary theory, but
    also of practical applications in medicine and bioengineering. Understanding this
    relationship is complicated by the ubiquitous phenomenon of epistasis, wherein
    mutation effects are dependent on their genetic context. Fitness landscapes —
    representations of phenotype as a function of genotype — are being increasingly
    used as a tool to study the effects and interactions of thousands of mutations,
    but are experimentally limited to exploring a small fraction of a protein’s theoretical
    sequence space. Furthermore, not all regions of said sequence space are necessarily
    equally informative. Thus, gene selection for landscape surveys should be carefully
    considered in order to maximize the usable output of necessarily limited data.\r\n\r\nIn
    this work, we analyzed the fitness landscapes of orthologous green fluorescent
    proteins from four different species, by systematically measuring the phenotype,
    fluorescence, of tens of thousands of mutant genotypes from each protein. These
    landscapes were highly heterogeneous, with some genes being mutationally robust
    and displaying epistasis only rarely, and others being highly epistatic and mutationally
    fragile. We used this data to train machine learning models to predict fluorescence
    from genotype. Although the training data contained almost exclusively genotypes
    with less than 3% sequence divergence from the original wild-type sequences, we
    were able to create novel, functional genotypes with up to 20% sequence divergence.
    Counterintuitively however, genes with high mutational robustness and rare epistasis
    were more difficult to introduce large numbers of mutations into, not less. This
    represents the first study of large-scale fitness landscapes of a protein family,
    and provides insights into how to approach future landscape surveys and their
    applications in novel protein design."
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
- _id: ScienComp
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Louisa
  full_name: Gonzalez Somermeyer, Louisa
  id: 4720D23C-F248-11E8-B48F-1D18A9856A87
  last_name: Gonzalez Somermeyer
  orcid: 0000-0001-9139-5383
citation:
  ama: Gonzalez Somermeyer L. Fitness landscapes of orthologous green fluorescent
    proteins. 2024. doi:<a href="https://doi.org/10.15479/at:ista:17850">10.15479/at:ista:17850</a>
  apa: Gonzalez Somermeyer, L. (2024). <i>Fitness landscapes of orthologous green
    fluorescent proteins</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:17850">https://doi.org/10.15479/at:ista:17850</a>
  chicago: Gonzalez Somermeyer, Louisa. “Fitness Landscapes of Orthologous Green Fluorescent
    Proteins.” Institute of Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:17850">https://doi.org/10.15479/at:ista:17850</a>.
  ieee: L. Gonzalez Somermeyer, “Fitness landscapes of orthologous green fluorescent
    proteins,” Institute of Science and Technology Austria, 2024.
  ista: Gonzalez Somermeyer L. 2024. Fitness landscapes of orthologous green fluorescent
    proteins. Institute of Science and Technology Austria.
  mla: Gonzalez Somermeyer, Louisa. <i>Fitness Landscapes of Orthologous Green Fluorescent
    Proteins</i>. Institute of Science and Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:17850">10.15479/at:ista:17850</a>.
  short: L. Gonzalez Somermeyer, Fitness Landscapes of Orthologous Green Fluorescent
    Proteins, Institute of Science and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-09-06T12:57:44Z
date_published: 2024-09-06T00:00:00Z
date_updated: 2026-04-07T13:25:01Z
day: '06'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: FyKo
doi: 10.15479/at:ista:17850
ec_funded: 1
file:
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  relation: source_file
file_date_updated: 2024-09-27T10:34:34Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '89'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
- _id: 26580278-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '771209'
  name: Characterizing the fitness landscape on population and global scales
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  link:
  - relation: software
    url: https://github.com/aequorea238/Orthologous_GFP_Fitness_Peaks
  record:
  - id: '11448'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Fyodor
  full_name: Kondrashov, Fyodor
  id: 44FDEF62-F248-11E8-B48F-1D18A9856A87
  last_name: Kondrashov
  orcid: 0000-0001-8243-4694
title: Fitness landscapes of orthologous green fluorescent proteins
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    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '18076'
abstract:
- lang: eng
  text: "The new era of Ge has opened up new possibilities in quantum computing. The
    maturity of Ge\r\nspin qubits is unquestioned, while hybrid semiconductor-superconductor
    Ge circuits are on track\r\nto enter the game. Gate-tunable transmons (gatemons)
    employing semiconductor Josephson\r\njunctions have recently emerged as building
    blocks for such hybrid quantum circuits. In this\r\nthesis, we present a gatemon
    fabricated in planar Germanium. We induce superconductivity\r\nin a two-dimensional
    hole gas by evaporating aluminum atop a thin spacer, which separates\r\nthe superconductor
    from the Ge quantum well. The Josephson junction is then integrated\r\ninto an
    Xmon circuit and capacitively coupled to a transmission line resonator. We showcase\r\nthe
    qubit tunability in a broad frequency range with resonator and two-tone spectroscopy.\r\nTime-domain
    characterizations reveal energy relaxation and coherence times up to 75 ns. Our\r\nresults,
    combined with the recent advances in the spin qubit field, pave the way towards
    novel\r\nhybrid and protected qubits in a group IV, CMOS-compatible material."
acknowledged_ssus:
- _id: NanoFab
- _id: M-Shop
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Oliver
  full_name: Sagi, Oliver
  id: 71616374-A8E9-11E9-A7CA-09ECE5697425
  last_name: Sagi
citation:
  ama: Sagi O. Hybrid circuits on planar Germanium. 2024. doi:<a href="https://doi.org/10.15479/at:ista:18076">10.15479/at:ista:18076</a>
  apa: Sagi, O. (2024). <i>Hybrid circuits on planar Germanium</i>. Institute of Science
    and Technology Austria. <a href="https://doi.org/10.15479/at:ista:18076">https://doi.org/10.15479/at:ista:18076</a>
  chicago: Sagi, Oliver. “Hybrid Circuits on Planar Germanium.” Institute of Science
    and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:18076">https://doi.org/10.15479/at:ista:18076</a>.
  ieee: O. Sagi, “Hybrid circuits on planar Germanium,” Institute of Science and Technology
    Austria, 2024.
  ista: Sagi O. 2024. Hybrid circuits on planar Germanium. Institute of Science and
    Technology Austria.
  mla: Sagi, Oliver. <i>Hybrid Circuits on Planar Germanium</i>. Institute of Science
    and Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:18076">10.15479/at:ista:18076</a>.
  short: O. Sagi, Hybrid Circuits on Planar Germanium, Institute of Science and Technology
    Austria, 2024.
corr_author: '1'
date_created: 2024-09-16T12:58:36Z
date_published: 2024-09-18T00:00:00Z
date_updated: 2026-04-16T12:20:39Z
day: '18'
ddc:
- '539'
degree_awarded: PhD
department:
- _id: GradSch
- _id: GeKa
doi: 10.15479/at:ista:18076
ec_funded: 1
file:
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  checksum: d01d0e2846c2f3ac5bb14d321554a4cd
  content_type: application/pdf
  creator: osagi
  date_created: 2024-09-18T14:13:01Z
  date_updated: 2024-09-18T14:13:01Z
  file_id: '18093'
  file_name: OliverSagi_Thesis_pdfa.pdf
  file_size: 86679095
  relation: main_file
  success: 1
- access_level: local
  checksum: 0543f473d509ee545f4ed3a56f742f4b
  content_type: application/x-zip-compressed
  creator: osagi
  date_created: 2024-09-18T14:14:02Z
  date_updated: 2024-09-19T09:20:33Z
  file_id: '18094'
  file_name: Thesis_OliverSagi.zip
  file_size: 172098524
  relation: source_file
file_date_updated: 2024-09-19T09:20:33Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '111'
project:
- _id: bd8bd29e-d553-11ed-ba76-f0070d4b237a
  grant_number: P36507
  name: Merging spin and superconducting qubits in planar Ge
- _id: c0977eea-5a5b-11eb-8a69-a862db0cf4d1
  grant_number: I05060
  name: High impedance circuit quantum electrodynamics with hole spins
- _id: 262116AA-B435-11E9-9278-68D0E5697425
  name: Hybrid Semiconductor - Superconductor Quantum Devices
- _id: 237E5020-32DE-11EA-91FC-C7463DDC885E
  call_identifier: H2020
  grant_number: '862046'
  name: TOPOLOGICALLY PROTECTED AND SCALABLE QUANTUM BITS
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '17202'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Georgios
  full_name: Katsaros, Georgios
  id: 38DB5788-F248-11E8-B48F-1D18A9856A87
  last_name: Katsaros
  orcid: 0000-0001-8342-202X
title: Hybrid circuits on planar Germanium
tmp:
  image: /images/cc_by_nc_sa.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC
    BY-NC-SA 4.0)
  short: CC BY-NC-SA (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '18088'
abstract:
- lang: eng
  text: "Instant messaging applications like Whatsapp, Signal or Telegram have become
    ubiquitous in today's society.\r\nMany of them provide not only end-to-end encryption,
    but also security guarantees even when the key material gets compromised.\r\nThese
    are achieved through frequent key update performed by users.\r\nIn particular,
    the compromise of a group key should preserve confidentiality of previously exchanged
    messages (forward secrecy), and a subsequent key update will ensure security for
    future ones (post-compromise security).\r\nThough great protocols for one-on-one
    communication have been known for some time, the design of ones that scale efficiently
    for larger groups while achieving akin security guarantees is a hard problem.\r\nA
    great deal of research has been aimed at this topic, much of it under the umbrella
    of the Messaging Layer Security (MLS) working group at the IETF. \r\nStarted in
    2018, this joint effort by academics and industry culminated in 2023 with the
    publication of the first standard for secure group messaging [IETF, RFC9420].\r\n\r\nAt
    the core of secure group messaging is a cryptographic primitive termed Continuous
    Group Key Agreement, or CGKA [Alwen et al. 2021], that essentially allows a changing
    group of users to agree on a common key with the added functionality security
    against compromises is achieved by users asynchronously issuing a key update.
    In this thesis we contribute to the understanding of CGKA across different angles.\r\nFirst,
    we present a new technique to effect dynamic operations in groups, i.e., add or
    remove members, that can be more efficient that the one employed by MLS in certain
    settings.\r\nConsidering the setting of users belonging to multiple overlapping
    groups, we then show lowerbounds on the communication cost of constructions that
    leverage said overlap, at the same time showing protocols that are asymptotically
    optimal and efficient for practical settings, respectively. Along the way, we
    show that the communication cost of key updates in MLS is average-cost optimal.\r\nAn
    important feature in CGKA protocols, particularly for big groups, is the possibility
    of executing several group operations concurrently. While later versions of MLS
    support this, they do at the cost of worsening the communication efficiency of
    future group operations.\r\nIn this thesis we introduce two new protocols that
    permit concurrency without any negative effect on efficiency. Our protocols circumvent
    previously existing lower bounds by satisfying a new notion of post-compromise
    security that only asks for security to be re-established after a certain number
    of key updates have taken place. While this can be slower than MLS in terms of
    rounds of communication, we show that it leads to more efficient overall communication.
    \r\nAdditionally, we introduce a new technique that allows group members to decrease
    the information they need to store and download, which makes one of our protocols
    enjoy much lower download cost than any other existing CGKA constructions. "
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Guillermo
  full_name: Pascual Perez, Guillermo
  id: 2D7ABD02-F248-11E8-B48F-1D18A9856A87
  last_name: Pascual Perez
  orcid: 0000-0001-8630-415X
citation:
  ama: Pascual Perez G. On the efficiency and security of secure group messaging.
    2024. doi:<a href="https://doi.org/10.15479/at:ista:18088">10.15479/at:ista:18088</a>
  apa: Pascual Perez, G. (2024). <i>On the efficiency and security of secure group
    messaging</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:18088">https://doi.org/10.15479/at:ista:18088</a>
  chicago: Pascual Perez, Guillermo. “On the Efficiency and Security of Secure Group
    Messaging.” Institute of Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:18088">https://doi.org/10.15479/at:ista:18088</a>.
  ieee: G. Pascual Perez, “On the efficiency and security of secure group messaging,”
    Institute of Science and Technology Austria, 2024.
  ista: Pascual Perez G. 2024. On the efficiency and security of secure group messaging.
    Institute of Science and Technology Austria.
  mla: Pascual Perez, Guillermo. <i>On the Efficiency and Security of Secure Group
    Messaging</i>. Institute of Science and Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:18088">10.15479/at:ista:18088</a>.
  short: G. Pascual Perez, On the Efficiency and Security of Secure Group Messaging,
    Institute of Science and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-09-18T12:59:49Z
date_published: 2024-09-18T00:00:00Z
date_updated: 2026-04-07T13:01:26Z
day: '18'
ddc:
- '000'
degree_awarded: PhD
department:
- _id: KrPi
- _id: GradSch
doi: 10.15479/at:ista:18088
ec_funded: 1
file:
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  checksum: ce0dca715b3df48e52e2e891b6ac1bc5
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  date_created: 2024-09-19T12:35:38Z
  date_updated: 2024-09-19T12:35:38Z
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  file_name: thesis_bundle.zip
  file_size: 11917734
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  date_created: 2024-09-19T12:36:08Z
  date_updated: 2024-09-19T12:36:08Z
  file_id: '18100'
  file_name: thesis_gpasper.pdf
  file_size: 2729427
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file_date_updated: 2024-09-19T12:36:08Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '239'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '10408'
    relation: part_of_dissertation
    status: public
  - id: '11476'
    relation: part_of_dissertation
    status: public
  - id: '18086'
    relation: part_of_dissertation
    status: public
  - id: '10049'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Krzysztof Z
  full_name: Pietrzak, Krzysztof Z
  id: 3E04A7AA-F248-11E8-B48F-1D18A9856A87
  last_name: Pietrzak
  orcid: 0000-0002-9139-1654
title: On the efficiency and security of secure group messaging
tmp:
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  short: CC BY-NC-SA (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '18132'
abstract:
- lang: eng
  text: "In this thesis, we are dealing with both arithmetic and geometric problems
    coming from the\r\nstudy of rational points with a particular focus on function
    fields over finite fields:\r\n(1) Using the circle method we produce upper bounds
    for the number of rational points of\r\nbounded height on diagonal cubic surfaces
    and fourfolds over Fq(t). This is based on\r\njoint work with Leonhard Hochfilzer.\r\n(2)
    We study rational points on smooth complete intersections X defined by cubic and\r\nquadratic
    hypersurfaces over Fq(t). We refine the Farey dissection of the “unit square”\r\ndeveloped
    by Vishe [202] and use the circle method with a Kloosterman refinement to\r\nestablish
    an asymptotic formula for the number of rational points of bounded height on\r\nX
    when dim(X) ≥ 23. Under the same hypotheses, we also verify weak approximation.\r\n(3)
    In joint work with Hochfilzer, we obtain upper bounds for the number of rational
    points of\r\nbounded height on del Pezzo surfaces of low degree over any global
    field. Our approach\r\nis to take hyperplane sections, which reduces the problem
    to uniform estimates for the\r\nnumber of rational points on curves.\r\n(4) We
    develop a version of the circle method capable of counting Fq-points on jet schemes\r\nof
    moduli spaces of rational curves on hypersurfaces. Combining this with a spreading\r\nout
    argument and a result of Mustaţă [150], this allows us to show that these moduli\r\nspaces
    only have canonical singularities under suitable assumptions on the degree and
    the\r\ndimension.\r\nIn addition, we give an overview of guiding questions and
    conjectures in the field of rational\r\npoints and explain the basic mechanism
    underlying the circle method.\r\n"
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Jakob
  full_name: Glas, Jakob
  id: d6423cba-dc74-11ea-a0a7-ee61689ff5fb
  last_name: Glas
citation:
  ama: Glas J. Counting rational points over function fields. 2024. doi:<a href="https://doi.org/10.15479/at:ista:18132">10.15479/at:ista:18132</a>
  apa: Glas, J. (2024). <i>Counting rational points over function fields</i>. Institute
    of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:18132">https://doi.org/10.15479/at:ista:18132</a>
  chicago: Glas, Jakob. “Counting Rational Points over Function Fields.” Institute
    of Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:18132">https://doi.org/10.15479/at:ista:18132</a>.
  ieee: J. Glas, “Counting rational points over function fields,” Institute of Science
    and Technology Austria, 2024.
  ista: Glas J. 2024. Counting rational points over function fields. Institute of
    Science and Technology Austria.
  mla: Glas, Jakob. <i>Counting Rational Points over Function Fields</i>. Institute
    of Science and Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:18132">10.15479/at:ista:18132</a>.
  short: J. Glas, Counting Rational Points over Function Fields, Institute of Science
    and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-09-23T18:58:08Z
date_published: 2024-09-23T00:00:00Z
date_updated: 2026-04-07T12:53:54Z
day: '23'
ddc:
- '512'
degree_awarded: PhD
department:
- _id: GradSch
- _id: TiBr
doi: 10.15479/at:ista:18132
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has_accepted_license: '1'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc/4.0/
month: '09'
oa: 1
oa_version: Published Version
page: '195'
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- _id: bd8a4fdc-d553-11ed-ba76-80a0167441a3
  grant_number: P36278
  name: Rational curves via function field analytic number theory
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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  - id: '18173'
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    status: public
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supervisor:
- first_name: Timothy D
  full_name: Browning, Timothy D
  id: 35827D50-F248-11E8-B48F-1D18A9856A87
  last_name: Browning
  orcid: 0000-0002-8314-0177
title: Counting rational points over function fields
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...
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OA_place: publisher
_id: '18135'
abstract:
- lang: eng
  text: "This thesis consists of two separate parts. In the first part we consider
    a dilute Fermi gas interacting through a repulsive interaction in dimensions $d=1,2,3$.
    Our focus is mostly on the physically most relevant dimension $d=3$ \r\nand the
    setting of a spin-polarized (equivalently spinless) gas, where the Pauli exclusion
    principle plays a key role. We show that, at zero temperature, the ground state
    energy density of the interacting spin-polarized gas differs (to leading order)
    from that of the free (i.e. non-interacting) gas by a term of order $a_p^d\\rho^{2+2/d}$
    \ with $a_p$ the $p$-wave scattering length of the repulsive interaction and $\\rho$
    the density. Further, we extend this to positive temperature and show that the
    pressure of an interacting spin-polarized gas differs from that of the free gas
    by a now temperature dependent term, again of order $a_p^d\\rho^{2+2/d}$. Lastly,
    we consider the setting of a spin-$\\frac{1}{2}$ Fermi gas in $d=3$ dimensions
    and show that here, as an upper bound, the ground state energy density differs
    from that of the free system by a term of order $a_s \\rho^2$ with an error smaller
    than $a_s \\rho^2 (a_s\\rho^{1/3})^{1-\\eps}$ for any $\\eps > 0$, where $a_s$
    is the $s$-wave scattering length of the repulsive interaction. \r\n\r\nThese
    asymptotic formulas complement the similar formulas in the literature for the
    dilute Bose and spin-$\\frac{1}{2}$ Fermi gas, where the ground state energies
    or pressures differ from that of the corresponding free systems by a term of order
    $a_s \\rho^2$ in dimension $d=3$. In the spin-polarized setting, the corrections,
    of order $a_p^3\\rho^{8/3}$ in dimension $d=3$, are thus much smaller and requires
    a more delicate analysis.\r\n\r\nIn the second part of the thesis we consider
    the Bardeen--Cooper--Schrieffer (BCS) theory of superconductivity and in particular
    its associated critical temperature and energy gap. We prove that the ratio of
    the zero-temperature energy gap and critical temperature $\\Xi(T=0)/T_c$ approaches
    a universal constant $\\pi e^{-\\gamma}\\approx 1.76$ in both the limit of high
    density in dimension $d=3$ and in the limit of weak coupling in dimensions $d=1,2$.
    This complements the proofs in the literature of this universal behaviour in the
    limit of weak coupling or low density in dimension $d=3$. Secondly, we prove that
    the ratio of the energy gap at positive temperature and critical temperature $\\Xi(T)/T_c$
    approaches a universal function of the relative temperature $T/T_c$ in the limit
    of weak coupling in dimensions $d=1,2,3$."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Asbjørn Bækgaard
  full_name: Lauritsen, Asbjørn Bækgaard
  id: e1a2682f-dc8d-11ea-abe3-81da9ac728f1
  last_name: Lauritsen
  orcid: 0000-0003-4476-2288
citation:
  ama: Lauritsen AB. Energies of dilute Fermi gases and universalities in BCS theory.
    2024. doi:<a href="https://doi.org/10.15479/at:ista:18135">10.15479/at:ista:18135</a>
  apa: Lauritsen, A. B. (2024). <i>Energies of dilute Fermi gases and universalities
    in BCS theory</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:18135">https://doi.org/10.15479/at:ista:18135</a>
  chicago: Lauritsen, Asbjørn Bækgaard. “Energies of Dilute Fermi Gases and Universalities
    in BCS Theory.” Institute of Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:18135">https://doi.org/10.15479/at:ista:18135</a>.
  ieee: A. B. Lauritsen, “Energies of dilute Fermi gases and universalities in BCS
    theory,” Institute of Science and Technology Austria, 2024.
  ista: Lauritsen AB. 2024. Energies of dilute Fermi gases and universalities in BCS
    theory. Institute of Science and Technology Austria.
  mla: Lauritsen, Asbjørn Bækgaard. <i>Energies of Dilute Fermi Gases and Universalities
    in BCS Theory</i>. Institute of Science and Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:18135">10.15479/at:ista:18135</a>.
  short: A.B. Lauritsen, Energies of Dilute Fermi Gases and Universalities in BCS
    Theory, Institute of Science and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-09-24T10:56:25Z
date_published: 2024-09-23T00:00:00Z
date_updated: 2026-04-16T08:17:55Z
day: '23'
ddc:
- '515'
- '539'
degree_awarded: PhD
department:
- _id: GradSch
- _id: RoSe
doi: 10.15479/at:ista:18135
ec_funded: 1
file:
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file_date_updated: 2024-09-26T13:12:55Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '353'
project:
- _id: bda63fe5-d553-11ed-ba76-a16e3d2f256b
  grant_number: I06427
  name: Mathematical Challenges in BCS Theory of Superconductivity
- _id: 25C6DC12-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '694227'
  name: Analysis of quantum many-body systems
publication_identifier:
  isbn:
  - 978-3-99078-042-8
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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    relation: part_of_dissertation
    status: public
  - id: '14542'
    relation: part_of_dissertation
    status: public
  - id: '18107'
    relation: part_of_dissertation
    status: public
  - id: '17240'
    relation: part_of_dissertation
    status: public
  - id: '14931'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
title: Energies of dilute Fermi gases and universalities in BCS theory
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  short: CC BY (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
OA_type: free access
_id: '18443'
abstract:
- lang: eng
  text: "In [KW06] Kapustin and Witten conjectured that there is a mirror symmetry
    relation between\r\nthe hyperkähler structures on certain Higgs bundle moduli
    spaces. As a consequence, they\r\nconjecture an equivalence between categories
    of BBB and BAA-branes. At the classical\r\nlevel, this mirror symmetry is given
    by T-duality between semi-flat hyperkähler structures on\r\nalgebraic integrable
    systems.\r\nIn this thesis, we investigate the T-duality relation between hyperkähler
    structures and the\r\ncorresponding branes on affine torus bundles. We use the
    techniques of generalized geometry\r\nto show that semi-flat hyperkähler structures
    are T-dual on algebraic integrable systems.\r\nWe also describe T-duality for
    generalized branes. Motivated by Fourier-Mukai transform\r\nwe upgrade the T-duality
    between generalized branes to T-duality of submanifolds endowed\r\nwith U(1)-bundles
    and connections. This T-duality in the appropriate context specializes to\r\nT-duality
    between BBB and BAA-branes.\r\n"
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Maria A
  full_name: Sisak, Maria A
  id: 44A03D04-AEA4-11E9-B225-EA2DE6697425
  last_name: Sisak
citation:
  ama: Sisak MA. T-dual branes on hyperkähler manifolds. 2024. doi:<a href="https://doi.org/10.15479/at:ista:18443">10.15479/at:ista:18443</a>
  apa: Sisak, M. A. (2024). <i>T-dual branes on hyperkähler manifolds</i>. Institute
    of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:18443">https://doi.org/10.15479/at:ista:18443</a>
  chicago: Sisak, Maria A. “T-Dual Branes on Hyperkähler Manifolds.” Institute of
    Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:18443">https://doi.org/10.15479/at:ista:18443</a>.
  ieee: M. A. Sisak, “T-dual branes on hyperkähler manifolds,” Institute of Science
    and Technology Austria, 2024.
  ista: Sisak MA. 2024. T-dual branes on hyperkähler manifolds. Institute of Science
    and Technology Austria.
  mla: Sisak, Maria A. <i>T-Dual Branes on Hyperkähler Manifolds</i>. Institute of
    Science and Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:18443">10.15479/at:ista:18443</a>.
  short: M.A. Sisak, T-Dual Branes on Hyperkähler Manifolds, Institute of Science
    and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-10-19T12:00:37Z
date_published: 2024-10-24T00:00:00Z
date_updated: 2026-04-07T12:42:44Z
day: '24'
ddc:
- '516'
degree_awarded: PhD
department:
- _id: GradSch
- _id: TaHa
doi: 10.15479/at:ista:18443
file:
- access_level: open_access
  checksum: 8c4893e726aaa4b3efb82758da9b6851
  content_type: application/pdf
  creator: msisak
  date_created: 2024-10-23T14:42:45Z
  date_updated: 2024-10-23T14:42:45Z
  file_id: '18467'
  file_name: MASisak_dissertation.pdf
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  date_updated: 2024-10-24T08:09:13Z
  file_id: '18468'
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  file_size: 617913
  relation: source_file
file_date_updated: 2024-10-24T08:09:13Z
has_accepted_license: '1'
keyword:
- hyperkaehler geometry
- branes
- mirror symmetry
- T-duality
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: '178'
project:
- _id: 6286e8c4-2b32-11ec-9570-f5297902f67f
  grant_number: '26069'
  name: Branes on hyperkÃ¤hler manifolds
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Tamás
  full_name: Hausel, Tamás
  id: 4A0666D8-F248-11E8-B48F-1D18A9856A87
  last_name: Hausel
  orcid: 0000-0002-9582-2634
title: T-dual branes on hyperkähler manifolds
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '17485'
abstract:
- lang: eng
  text: "Large language models (LLMs) have made tremendous progress in the past few
    years, from being able to generate coherent text to matching or surpassing humans
    in a wide variety of creative, knowledge or reasoning tasks. Much of this can
    be attributed to massively increased scale, both in the size of the model as well
    as the amount of training data, from 100s of millions to 100s of billions, or
    even trillions. This trend is expected to continue, which, although exciting,
    also raises major practical concerns. Already today's 100+ billion parameter LLMs
    require top-of-the-line hardware just to run. Hence, it is clear that sustaining
    these developments will require significant efficiency advances.\r\n\r\nHistorically,
    one of the most practical ways of improving model efficiency has been compression,
    especially in the form of sparsity or quantization. While this has been studied
    extensively in the past, existing accurate methods are all designed for models
    around 100 million parameters; scaling them up to ones literally 1000x larger
    is highly challenging. In this thesis, we introduce a new unified sparsification
    and quantization approach OBC, which through additional algorithmic enhancements
    leads to GPTQ and SparseGPT, the first techniques fast and accurate enough to
    compress 100+ billion parameter models to 4- or even 3-bit precision and 50% weight-sparsity,
    respectively. Additionally, we show how weight-only quantizion does not just bring
    space savings but also up to 4.5x faster generation speed, via custom GPU kernels.\r\n\r\nIn
    fact, we show for the first time that it is possible to develop an FP16 times
    INT4 mixed-precision matrix multiplication kernel, called Marlin, which comes
    close to simultaneously maximizing both memory and compute utilization, making
    weight-only quantization highly practical even for multi-user serving. Further,
    we demonstrate that GPTQ can be scaled to widely overparametrized trillion-parameter
    models, where extreme sub-1-bit compression rates can be achieved without any
    inference slow-down, by co-designing a bespoke entropy coding scheme together
    with an efficient kernel.\r\n\r\nFinally, we also study compression from the perspective
    of someone with access to massive amounts of compute resources for training large
    models completely from scratch. Here the key questions evolve around the joint
    scaling behavior between compression, model size, and amount of training data
    used. Based on extensive experimental results for both vision and text models,
    we introduce the first scaling law which accurately captures the relationship
    between weight-sparsity, number of non-zero weights and data. This further allows
    us to characterize the optimal sparsity, which we find to increase the longer
    a fixed cost model is being trained.\r\n\r\nOverall, this thesis presents contributions
    to three different angles of large model efficiency: affordable but accurate algorithms,
    highly efficient systems implementations, and fundamental scaling laws for compressed
    training."
acknowledged_ssus:
- _id: ScienComp
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Elias
  full_name: Frantar, Elias
  id: 09a8f98d-ec99-11ea-ae11-c063a7b7fe5f
  last_name: Frantar
citation:
  ama: 'Frantar E. Compressing large neural networks : Algorithms, systems and scaling
    laws. 2024. doi:<a href="https://doi.org/10.15479/at:ista:17485">10.15479/at:ista:17485</a>'
  apa: 'Frantar, E. (2024). <i>Compressing large neural networks : Algorithms, systems
    and scaling laws</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:17485">https://doi.org/10.15479/at:ista:17485</a>'
  chicago: 'Frantar, Elias. “Compressing Large Neural Networks : Algorithms, Systems
    and Scaling Laws.” Institute of Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:17485">https://doi.org/10.15479/at:ista:17485</a>.'
  ieee: 'E. Frantar, “Compressing large neural networks : Algorithms, systems and
    scaling laws,” Institute of Science and Technology Austria, 2024.'
  ista: 'Frantar E. 2024. Compressing large neural networks : Algorithms, systems
    and scaling laws. Institute of Science and Technology Austria.'
  mla: 'Frantar, Elias. <i>Compressing Large Neural Networks : Algorithms, Systems
    and Scaling Laws</i>. Institute of Science and Technology Austria, 2024, doi:<a
    href="https://doi.org/10.15479/at:ista:17485">10.15479/at:ista:17485</a>.'
  short: 'E. Frantar, Compressing Large Neural Networks : Algorithms, Systems and
    Scaling Laws, Institute of Science and Technology Austria, 2024.'
corr_author: '1'
date_created: 2024-09-02T11:01:48Z
date_published: 2024-09-05T00:00:00Z
date_updated: 2026-07-07T13:22:38Z
day: '05'
ddc:
- '000'
degree_awarded: PhD
department:
- _id: GradSch
- _id: DaAl
doi: 10.15479/at:ista:17485
ec_funded: 1
file:
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file_date_updated: 2024-09-06T16:24:59Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '129'
project:
- _id: 268A44D6-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '805223'
  name: Elastic Coordination for Scalable Machine Learning
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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    relation: part_of_dissertation
    status: public
  - id: '18062'
    relation: part_of_dissertation
    status: public
  - id: '18061'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
title: 'Compressing large neural networks : Algorithms, systems and scaling laws'
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '18667'
abstract:
- lang: eng
  text: "Many chemical and physical properties of materials are determined by the
    material’s shape,\r\nfor example the size of its pores and the width of its tunnels.
    This makes materials science\r\na prime application area for geometrical and topological
    methods. Nevertheless many\r\nmethods in topological data analysis have not been
    satisfyingly extended to the needs of\r\nmaterials science. This thesis provides
    new methods and new mathematical theorems\r\ntargeted at those specific needs
    by answering four different research questions. While the\r\nmotivation for each
    of the research questions arises from materials science, the methods\r\nare versatile
    and can be applied in different areas as well. \r\n\r\nThe first research question
    is concerned with image data, for example a three-dimensional\r\ncomputed tomography
    (CT) scan of a material, like sand or stone. There are two commonly\r\nused topologies
    for digital images and depending on the application either of them might be\r\nrequired.
    However, software for computing the topological data analysis method persistence\r\nhomology,
    usually supports only one of the two topologies. We answer the question how to\r\ncompute
    persistent homology of an image with respect to one of the two topologies using\r\nsoftware
    that is intended for the other topology. \r\n\r\nThe second research question
    is concerned with image data as well, and asks how much\r\nof the topological
    information of an image is lost when the resolution is coarsened. As\r\ncomputer
    tomography scanners are more expensive the higher the resolution, it is an\r\nimportant
    question in materials science to know which resolution is enough to get satisfying\r\npersistent
    homology. We give theoretical bounds on the information loss based on different\r\ngeometrical
    properties of the object to be scanned. In addition, we conduct experiments on\r\nsand
    and stone CT image data. \r\n\r\nThe third research question is motivated by comparing
    crystalline materials efficiently. As\r\nthe atoms within a crystal repeat periodically,
    crystalline materials are either modeled by\r\nunmanageable infinite periodic
    point sets, or by one of their fundamental domains, which is\r\nunstable under
    perturbation. Therefore a fingerprint of crystalline materials is needed, with\r\nappropriate
    properties such that comparing the crystals can be eased by comparing the\r\nfingerprints
    instead. We define the density fingerprint and prove the necessary properties.
    \r\n\r\nThe fourth research question is motivated by studying the hole-structure
    or connectedness,\r\ni.e. persistent homology or merge trees, of crystalline materials.
    A common way to deal\r\nwith periodicity is to take a fundamental domain and identify
    opposite boundaries to form a\r\ntorus. However, computing persistent homology
    or merge trees on that torus loses some\r\nof the information materials scientists
    are interested in and is additionally not stable under\r\ncertain noise. We therefore
    decorate the merge tree stemming from the torus with additional\r\ninformation
    describing the density and growth rate of the periodic copies of a component\r\nwithin
    a growing spherical window. We prove all desired properties, like stability and
    efficient\r\ncomputability."
acknowledgement: "I was supported by the European Research Council (ERC) Horizon 2020
  project\r\n“Alpha Shape Theory Extended” No. 788183 and by the Pöttinger Scholarship.
  In addition,\r\nI am very thankful for having been able to attend the second Workshop
  for Women in\r\nComputational Topology in July 2019, funded by the Mathematical
  Sciences Institute at\r\nANU, the US National Science Foundation through the award
  CCF-1841455, the Australian\r\nMathematical Sciences Institute and the Association
  for Women in Mathematics. Two of the\r\nprojects presented in this thesis started
  there. One of them reached completion thanks to\r\nfunding from the MSRI Summer
  Research in Mathematics program awarded to me and my\r\ncollaborators in 2020."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Teresa
  full_name: Heiss, Teresa
  id: 4879BB4E-F248-11E8-B48F-1D18A9856A87
  last_name: Heiss
  orcid: 0000-0002-1780-2689
citation:
  ama: Heiss T. New methods for applying topological data analysis to materials science.
    2024. doi:<a href="https://doi.org/10.15479/at:ista:18667">10.15479/at:ista:18667</a>
  apa: Heiss, T. (2024). <i>New methods for applying topological data analysis to
    materials science</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:18667">https://doi.org/10.15479/at:ista:18667</a>
  chicago: Heiss, Teresa. “New Methods for Applying Topological Data Analysis to Materials
    Science.” Institute of Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:18667">https://doi.org/10.15479/at:ista:18667</a>.
  ieee: T. Heiss, “New methods for applying topological data analysis to materials
    science,” Institute of Science and Technology Austria, 2024.
  ista: Heiss T. 2024. New methods for applying topological data analysis to materials
    science. Institute of Science and Technology Austria.
  mla: Heiss, Teresa. <i>New Methods for Applying Topological Data Analysis to Materials
    Science</i>. Institute of Science and Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:18667">10.15479/at:ista:18667</a>.
  short: T. Heiss, New Methods for Applying Topological Data Analysis to Materials
    Science, Institute of Science and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-12-17T16:17:55Z
date_published: 2024-12-17T00:00:00Z
date_updated: 2026-07-07T13:43:27Z
day: '17'
ddc:
- '514'
- '516'
- '004'
degree_awarded: PhD
department:
- _id: GradSch
- _id: HeEd
doi: 10.15479/at:ista:18667
ec_funded: 1
file:
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keyword:
- persistent homology
- topological data analysis
- periodic
- crystalline materials
- images
- fingerprint
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: '111'
project:
- _id: 266A2E9E-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '788183'
  name: Alpha Shape Theory Extended
publication_identifier:
  isbn:
  - 978-3-99078-052-7
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
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  - id: '18673'
    relation: part_of_dissertation
    status: public
  - id: '9345'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Herbert
  full_name: Edelsbrunner, Herbert
  id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
  last_name: Edelsbrunner
  orcid: 0000-0002-9823-6833
title: New methods for applying topological data analysis to materials science
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type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '17225'
abstract:
- lang: eng
  text: "This thesis describes the development of an atom interferometer designed
    to exploit the\r\nadvantages of utilizing quantum entanglement for enhanced precision
    measurements beyond\r\nthe standard quantum limit. While the project remains ongoing,
    significant progress has been\r\nmade.\r\nA key contribution of this work is the
    development of Quantrol, an experimental control\r\nsystem leveraging the ARTIQ
    framework. This software enables precise timing and control\r\nwithout requiring
    prior knowledge of ARTIQ’s implementation details or coding experience.\r\nThe
    interface offers user friendly visual comprehension of the experimental sequence
    and\r\nextended capabilities, allowing researchers to scan variables with a simple
    click of a mouse.\r\nThe main proposed project is to implement atom interferometric
    sequence with squeezed input\r\nstates inside of a dipole trap generated by a
    high finesse cavity. The presence of the dipole\r\ntrap allows one dimensional
    atomic cloud split while maintaining relatively strong confinement\r\nin other
    directions.\r\nWe are currently able to trap and cool 87Rb atoms to few micro
    kelvin temperatures, load\r\nthem into the dipole trap and state prepare them
    to be used for squeezing and interferometric\r\nsequence."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Vyacheslav
  full_name: Li, Vyacheslav
  id: 3A4FAA92-F248-11E8-B48F-1D18A9856A87
  last_name: Li
citation:
  ama: Li V. Towards a quantum entanglement enhanced atom interferomter. 2024. doi:<a
    href="https://doi.org/10.15479/at:ista:17225">10.15479/at:ista:17225</a>
  apa: Li, V. (2024). <i>Towards a quantum entanglement enhanced atom interferomter</i>.
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:17225">https://doi.org/10.15479/at:ista:17225</a>
  chicago: Li, Vyacheslav. “Towards a Quantum Entanglement Enhanced Atom Interferomter.”
    Institute of Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:17225">https://doi.org/10.15479/at:ista:17225</a>.
  ieee: V. Li, “Towards a quantum entanglement enhanced atom interferomter,” Institute
    of Science and Technology Austria, 2024.
  ista: Li V. 2024. Towards a quantum entanglement enhanced atom interferomter. Institute
    of Science and Technology Austria.
  mla: Li, Vyacheslav. <i>Towards a Quantum Entanglement Enhanced Atom Interferomter</i>.
    Institute of Science and Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:17225">10.15479/at:ista:17225</a>.
  short: V. Li, Towards a Quantum Entanglement Enhanced Atom Interferomter, Institute
    of Science and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-07-11T09:46:48Z
date_published: 2024-07-11T00:00:00Z
date_updated: 2026-07-08T08:50:57Z
day: '11'
ddc:
- '530'
degree_awarded: PhD
department:
- _id: GradSch
- _id: OnHo
doi: 10.15479/at:ista:17225
file:
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file_date_updated: 2024-07-11T10:26:22Z
has_accepted_license: '1'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: '79'
project:
- _id: bdb2a702-d553-11ed-ba76-f12e3e5a3bc6
  grant_number: '101087907'
  name: 'A quantum hybrid of atoms and milligram-scale pendulums: towards gravitational
    quantum mechanics'
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '11438'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Onur
  full_name: Hosten, Onur
  id: 4C02D85E-F248-11E8-B48F-1D18A9856A87
  last_name: Hosten
  orcid: 0000-0002-2031-204X
title: Towards a quantum entanglement enhanced atom interferomter
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  short: CC BY-NC-SA (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '17119'
abstract:
- lang: eng
  text: "Genomes are shaped by natural selection at the level of the organism, as
    genomic variants that\r\nhave a beneficial effect on the viability or fecundity
    of their carriers are on average expected\r\nto be passed on to more offspring
    than less beneficial alleles. However, selection also favors\r\ngenomic variants
    that drive their own transmission to the next generation above the mendelian\r\nexpectation
    of 50 percent in heterozygotes, even if these self-promoting variants are less\r\nbeneficial
    to the organism than other variants at the same locus. Such variants, called meiotic\r\ndrivers,
    are found in diverse taxa, and often impose fitness costs on their host organisms.
    As\r\nmeiotic drivers often require multiple genes and sequences for transmission
    ratio distortion,\r\nthey are often found in regions of low recombination, such
    as inversions, which prevent their\r\nrecombination with the non-driving homologous
    regions. Reduced recombination rates are\r\nexpected to lead to the accumulation
    of deleterious mutations, which may affect hundreds\r\nof genes trapped in the
    inversions of meiotic drivers. Although the observed fitness costs of\r\nself-promoting
    haplotypes are thought to possibly reflect sequence degeneration, no study has\r\nsystematically
    investigated the level of degeneration on a meiotic driver. Further, the low\r\nrates
    of recombination between driving and non-driving haplotypes have limited the power
    of\r\ntraditional genetic studies in uncovering the gene content of meiotic drivers,
    and made the\r\nthe identification of the genes causing transmission ratio distortion
    difficult.\r\nAfter an introduction to meiotic drivers in Chapter 1, this thesis
    presents three studies that\r\nmake use of next generation sequencing data to
    characterize the sequence and expression\r\nevolution of genes on the t-haplotype,
    a large and ancient meiotic driver in house mice that is\r\ntransmitted to up
    to 100% of the offspring in males heterozygous for it. Chapter 2 presents\r\na
    comprehensive assessment of the t-haplotype’s sequence evolution, which shows
    signs of\r\nsequence degeneration counteracted by occasional recombination with
    the non-driving homolog\r\nover large parts of the meiotic driver, proposing an
    explanation for its long-term survival.\r\nChapter 3 investigates the sequence
    and expression evolution of genes on the t-haplotype,\r\nand finds widespread
    expression and copy number changes and signs of less efficient purifying\r\nselection
    compared to the genes on the non-driving homolog. Further, this chapter finds\r\ncandidates
    for involvment in drive: two positively selected genes on the t-haplotype, and\r\nthe
    discovery of a t-specific gene duplicate, which was gained from another chromosome,\r\nand
    which acquired novel sequence and testis-specific expression on the t-haplotype.
    Finally,\r\nChapter 4 provides unprecedented insights into the gene expression
    landscape in testes of\r\nt-carrier mice, using single nucleus sequencing. Cell-resolved
    RNA-sequencing allows the\r\ncomparison of expression in spermatids carrying or
    not carrying the t-haplotype as well as the\r\ntiming of t-haplotype-induced expression
    changes along spermatogenesis. This study shows\r\nthe timing of previously found
    drive-associated genes, and uncovers novel candidate genes and\r\nbiological processes
    that may underlie the complex biology of transmission ratio distortion of\r\nthe
    t-haplotype. Chapter 5 synthesizes the findings of the three studies, and discusses
    them in\r\nthe context of the current state of meiotic drive research."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Réka K
  full_name: Kelemen, Réka K
  id: 48D3F8DE-F248-11E8-B48F-1D18A9856A87
  last_name: Kelemen
  orcid: 0000-0002-8489-9281
citation:
  ama: Kelemen RK. Characterizing the sequence and expression evolution of the t-haplotype,
    a model meiotic driver. 2024. doi:<a href="https://doi.org/10.15479/at:ista:17119">10.15479/at:ista:17119</a>
  apa: Kelemen, R. K. (2024). <i>Characterizing the sequence and expression evolution
    of the t-haplotype, a model meiotic driver</i>. Institute of Science and Technology
    Austria. <a href="https://doi.org/10.15479/at:ista:17119">https://doi.org/10.15479/at:ista:17119</a>
  chicago: Kelemen, Réka K. “Characterizing the Sequence and Expression Evolution
    of the T-Haplotype, a Model Meiotic Driver.” Institute of Science and Technology
    Austria, 2024. <a href="https://doi.org/10.15479/at:ista:17119">https://doi.org/10.15479/at:ista:17119</a>.
  ieee: R. K. Kelemen, “Characterizing the sequence and expression evolution of the
    t-haplotype, a model meiotic driver,” Institute of Science and Technology Austria,
    2024.
  ista: Kelemen RK. 2024. Characterizing the sequence and expression evolution of
    the t-haplotype, a model meiotic driver. Institute of Science and Technology Austria.
  mla: Kelemen, Réka K. <i>Characterizing the Sequence and Expression Evolution of
    the T-Haplotype, a Model Meiotic Driver</i>. Institute of Science and Technology
    Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:17119">10.15479/at:ista:17119</a>.
  short: R.K. Kelemen, Characterizing the Sequence and Expression Evolution of the
    T-Haplotype, a Model Meiotic Driver, Institute of Science and Technology Austria,
    2024.
corr_author: '1'
date_created: 2024-06-07T16:14:13Z
date_published: 2024-06-20T00:00:00Z
date_updated: 2026-04-07T13:21:37Z
day: '20'
ddc:
- '576'
degree_awarded: PhD
department:
- _id: GradSch
- _id: BeVi
doi: 10.15479/at:ista:17119
ec_funded: 1
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keyword:
- meiotic driver
- neofunctionalization
- single nucleus sequencing
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
page: '105'
project:
- _id: 250BDE62-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '715257'
  name: Prevalence and Influence of Sexual Antagonism on Genome Evolution
- _id: 34ae1506-11ca-11ed-8bc3-c14f4c474396
  grant_number: F8810
  name: The highjacking of meiosis for asexual reproduction
publication_identifier:
  isbn:
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  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
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supervisor:
- first_name: Beatriz
  full_name: Vicoso, Beatriz
  id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
  last_name: Vicoso
  orcid: 0000-0002-4579-8306
title: Characterizing the sequence and expression evolution of the t-haplotype, a
  model meiotic driver
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  short: CC BY-NC-SA (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
_id: '18477'
abstract:
- lang: eng
  text: "ADAR1 is broadly expressed across various tissues and is vital in regulating
    pathways\r\nassociated with innate immune responses. ADAR1 marks double-stranded
    RNA as \"self\"\r\nthrough its A-to-I editing activity, effectively repressing
    autoimmunity and maintaining\r\nimmune tolerance. This editing process has been
    detected at millions of sites across the\r\nhuman genome. However, the mechanism
    underlying ADAR1's substrate selectivity\r\nproperties remains largely unclear,
    with much of the current knowledge derived from\r\ncomparisons to its more extensively
    studied homolog, ADAR2. By studying ADAR1 in complex\r\nwith its RNA substrates
    and applying a combination of biochemical techniques and structural\r\nstudies
    using CryoEM, we aim to gain a more comprehensive understanding of the substrate\r\nselectivity
    characteristics of ADAR1.\r\nIn this thesis, the purification protocol for ADAR1
    was successfully optimized, resulting in the\r\nfirst report in the literature
    to achieve high protein purity and activity. This advancement\r\nenabled the investigation
    of complex formation between ADAR1 and various RNA substrates,\r\nleading to the
    identification of optimal conditions for preparing the cryoEM sample. However,\r\ndespite
    comprehensive optimization of the cryo-EM conditions, the resulting data lacked
    the\r\ndesired quality, highlighting the need for similar rigorous optimization
    of the RNA substrates\r\nto facilitate structural studies of the ADAR1-RNA complex.
    The study was complemented by\r\nAlphaFold predictions, which provided some insights
    into this mechanism.\r\nMoreover, during this project I established a collaboration
    with a research group focused on\r\nstudying ADAR homologs. Notably ADAR homologs
    were identified in bivalve species, and it\r\nwas further demonstrated that ADAR
    and its A-to-I editing activity are upregulated in Pacific\r\noysters during infections
    with Ostreid herpesvirus-1—a highly infectious virus that leads to\r\nsignificant
    losses in oyster populations globally. I successfully purified oyster ADAR and\r\nprepared
    in vitro edited RNA for nanopore sequencing—a direct sequencing technology\r\ncapable
    of detecting modified nucleotides without the need for reverse transcription.
    The\r\ncollaborators initiated optimization of this nanopore-based approach. However,
    current\r\ntechnological limitations still constrain the reliable detection of
    modified nucleotides.\r\nThe project also examined the impact of RNA editing on
    RNA binding and filament formation\r\nby MDA5, a key cytosolic dsRNA sensor that
    triggers an interferon response. A primary target\r\nof ADAR1's editing activity
    is RNA derived from repetitive elements present in the genome,\r\nparticularly
    Alu elements forming double-stranded RNA. When unedited, these RNA\r\nsequences
    are recognized by MDA5. However, the mechanisms by which MDA5 interacts with\r\nAlu
    RNAs, as well as the role of A-to-I editing in influencing this binding, are still
    not well\r\nunderstood.\r\nThe interaction between MDA5 and Alu elements, was
    successfully established. This was\r\nachieved through the testing of different
    RNA variants and the evaluation of filament\r\nformation using binding techniques
    and electron microscopy imaging. This groundwork has\r\nset the conditions for
    further evaluation using CryoEM. Furthermore, the effects of A-to-I\r\nediting
    on the binding properties of MDA5 with Alu RNA were investigated. Given the recent\r\nresearch
    that has provided new insights into MDA5's interaction with dsRNA, it is essential
    to\r\nrevise the experimental setup to integrate these findings before moving
    forward with the\r\nCryoEM sample analysis."
acknowledged_ssus:
- _id: EM-Fac
- _id: LifeSc
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Beata M
  full_name: Kaczmarek, Beata M
  id: 36FA4AFA-F248-11E8-B48F-1D18A9856A87
  last_name: Kaczmarek
citation:
  ama: Kaczmarek BM. Biochemical and structural insights into ADAR1 RNA editing. 2024.
    doi:<a href="https://doi.org/10.15479/at:ista:18477">10.15479/at:ista:18477</a>
  apa: Kaczmarek, B. M. (2024). <i>Biochemical and structural insights into ADAR1
    RNA editing</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:18477">https://doi.org/10.15479/at:ista:18477</a>
  chicago: Kaczmarek, Beata M. “Biochemical and Structural Insights into ADAR1 RNA
    Editing.” Institute of Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:18477">https://doi.org/10.15479/at:ista:18477</a>.
  ieee: B. M. Kaczmarek, “Biochemical and structural insights into ADAR1 RNA editing,”
    Institute of Science and Technology Austria, 2024.
  ista: Kaczmarek BM. 2024. Biochemical and structural insights into ADAR1 RNA editing.
    Institute of Science and Technology Austria.
  mla: Kaczmarek, Beata M. <i>Biochemical and Structural Insights into ADAR1 RNA Editing</i>.
    Institute of Science and Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:18477">10.15479/at:ista:18477</a>.
  short: B.M. Kaczmarek, Biochemical and Structural Insights into ADAR1 RNA Editing,
    Institute of Science and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-10-27T07:35:13Z
date_published: 2024-10-29T00:00:00Z
date_updated: 2026-04-07T13:23:59Z
day: '29'
ddc:
- '572'
degree_awarded: PhD
department:
- _id: GradSch
- _id: CaBe
doi: 10.15479/at:ista:18477
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month: '10'
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page: '124'
publication_identifier:
  isbn:
  - 978-3-99078-045-9
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Carrie A
  full_name: Bernecky, Carrie A
  id: 2CB9DFE2-F248-11E8-B48F-1D18A9856A87
  last_name: Bernecky
  orcid: 0000-0003-0893-7036
title: Biochemical and structural insights into ADAR1 RNA editing
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
---
OA_place: publisher
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abstract:
- lang: eng
  text: "The hippocampus is central to memory formation, storage and retrieval over
    many\r\ntimescales. Neurons in this brain area are highly selective to spatial
    position as well as to many\r\nother variables of the environment. It is believed
    that the selectivity patterns of hippocampal\r\nneurons reflect the structure
    of tasks an animal performs. However, especially at timescales\r\nlonger than
    a few minutes or hours it is not fully known how these representations evolve,
    nor\r\nhow they map to behaviour in the process. In this thesis, I monitored the
    evolution of\r\nhippocampal representations in a novel spatial-associative memory
    task for rats. Reward\r\nlocations were associated with global sensory cues (i.e.
    context); animals had to remember the\r\nassociations and dig for food in those
    locations only. I used in vivo electrophysiology to record\r\nthe activity of
    the hippocampus dorsal CA1 neurons during the learning period of a few days.\r\nI
    report here a novel and simple method to classify behaviour performance to account\r\nfor
    individual variability in learning speed and spurious performance unrelated to
    true task rule\r\nlearning. Using this classification I was then able to investigate
    neural responses on different\r\nstages of learning matched across animals. On
    the first day of learning, I observed a fast\r\nformation of single-cell selectivity
    to task variables which remained stable over days. I also\r\nobserved that reward
    tuning was not a single process but dependent on task-related cognitive\r\nload.
    At the population level, a linear decoding approach revealed a hierarchy in the\r\nrepresentation
    of task variables that changed with learning. In the high-dimensional space of\r\npopulation
    activity, the representation of contexts was specific to each position in the
    maze, and\r\ncould thus be better decoded if the position was known. The decoding
    of position did not improve\r\nwith knowledge of other variables. As learning
    progressed, the hippocampal code underwent a\r\nreorganisation of high-variance
    directions in population activity, identified by principal\r\ncomponent analysis.
    I found that dominant dimensions started carrying increasing amounts of\r\ninformation
    about task context specifically at those positions where it mattered for task\r\nperformance.
    When I contrasted this with variables less relevant to task performance (e.g.\r\nmovement
    direction), I did not observe differences in decoding quality over positions nor
    a\r\nreduction of dimensionality with learning.\r\nOverall, the largest changes
    in CA1 neural response with task learning happened in a\r\nmatter of a few trials;
    over days, changes undetectable in single-cell statistics were responsible\r\nfor
    re-structuring the hierarchy of neural representations at the population level;
    these changes\r\nwere task-specific and reflected different stages of learning.
    This indicates that complex task\r\nlearning may involve different magnitudes
    of response modulation in CA1, which happen at\r\nspecific time scales linked
    to behaviour."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Heloisa
  full_name: Chiossi, Heloisa
  id: 2BBA502C-F248-11E8-B48F-1D18A9856A87
  last_name: Chiossi
  orcid: 0009-0004-2973-278X
citation:
  ama: Chiossi HSC. Adaptive hierarchical representations in the hippocampus. 2024.
    doi:<a href="https://doi.org/10.15479/at:ista:14821">10.15479/at:ista:14821</a>
  apa: Chiossi, H. S. C. (2024). <i>Adaptive hierarchical representations in the hippocampus</i>.
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:14821">https://doi.org/10.15479/at:ista:14821</a>
  chicago: Chiossi, Heloisa S. C. “Adaptive Hierarchical Representations in the Hippocampus.”
    Institute of Science and Technology Austria, 2024. <a href="https://doi.org/10.15479/at:ista:14821">https://doi.org/10.15479/at:ista:14821</a>.
  ieee: H. S. C. Chiossi, “Adaptive hierarchical representations in the hippocampus,”
    Institute of Science and Technology Austria, 2024.
  ista: Chiossi HSC. 2024. Adaptive hierarchical representations in the hippocampus.
    Institute of Science and Technology Austria.
  mla: Chiossi, Heloisa S. C. <i>Adaptive Hierarchical Representations in the Hippocampus</i>.
    Institute of Science and Technology Austria, 2024, doi:<a href="https://doi.org/10.15479/at:ista:14821">10.15479/at:ista:14821</a>.
  short: H.S.C. Chiossi, Adaptive Hierarchical Representations in the Hippocampus,
    Institute of Science and Technology Austria, 2024.
corr_author: '1'
date_created: 2024-01-16T14:25:21Z
date_published: 2024-01-19T00:00:00Z
date_updated: 2026-04-07T13:21:56Z
day: '19'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JoCs
doi: 10.15479/at:ista:14821
ec_funded: 1
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has_accepted_license: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: '89'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Jozsef L
  full_name: Csicsvari, Jozsef L
  id: 3FA14672-F248-11E8-B48F-1D18A9856A87
  last_name: Csicsvari
  orcid: 0000-0002-5193-4036
title: Adaptive hierarchical representations in the hippocampus
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2024'
...
