@article{7210,
  abstract     = {The rate of biological evolution depends on the fixation probability and on the fixation time of new mutants. Intensive research has focused on identifying population structures that augment the fixation probability of advantageous mutants. But these amplifiers of natural selection typically increase fixation time. Here we study population structures that achieve a tradeoff between fixation probability and time. First, we show that no amplifiers can have an asymptotically lower absorption time than the well-mixed population. Then we design population structures that substantially augment the fixation probability with just a minor increase in fixation time. Finally, we show that those structures enable higher effective rate of evolution than the well-mixed population provided that the rate of generating advantageous mutants is relatively low. Our work sheds light on how population structure affects the rate of evolution. Moreover, our structures could be useful for lab-based, medical, or industrial applications of evolutionary optimization.},
  author       = {Tkadlec, Josef and Pavlogiannis, Andreas and Chatterjee, Krishnendu and Nowak, Martin A.},
  issn         = {2399-3642},
  journal      = {Communications Biology},
  publisher    = {Springer Nature},
  title        = {{Population structure determines the tradeoff between fixation probability and fixation time}},
  doi          = {10.1038/s42003-019-0373-y},
  volume       = {2},
  year         = {2019},
}

@article{7214,
  abstract     = {Background: Many cancer genomes are extensively rearranged with highly aberrant chromosomal karyotypes. Structural and copy number variations in cancer genomes can be determined via abnormal mapping of sequenced reads to the reference genome. Recently it became possible to reconcile both of these types of large-scale variations into a karyotype graph representation of the rearranged cancer genomes. Such a representation, however, does not directly describe the linear and/or circular structure of the underlying rearranged cancer chromosomes, thus limiting possible analysis of cancer genomes somatic evolutionary process as well as functional genomic changes brought by the large-scale genome rearrangements.

Results: Here we address the aforementioned limitation by introducing a novel methodological framework for recovering rearranged cancer chromosomes from karyotype graphs. For a cancer karyotype graph we formulate an Eulerian Decomposition Problem (EDP) of finding a collection of linear and/or circular rearranged cancer chromosomes that are determined by the graph. We derive and prove computational complexities for several variations of the EDP. We then demonstrate that Eulerian decomposition of the cancer karyotype graphs is not always unique and present the Consistent Contig Covering Problem (CCCP) of recovering unambiguous cancer contigs from the cancer karyotype graph, and describe a novel algorithm CCR capable of solving CCCP in polynomial time. We apply CCR on a prostate cancer dataset and demonstrate that it is capable of consistently recovering large cancer contigs even when underlying cancer genomes are highly rearranged.

Conclusions: CCR can recover rearranged cancer contigs from karyotype graphs thereby addressing existing limitation in inferring chromosomal structures of rearranged cancer genomes and advancing our understanding of both patient/cancer-specific as well as the overall genetic instability in cancer.},
  author       = {Aganezov, Sergey and Zban, Ilya and Aksenov, Vitalii and Alexeev, Nikita and Schatz, Michael C.},
  issn         = {1471-2105},
  journal      = {BMC Bioinformatics},
  publisher    = {BMC},
  title        = {{Recovering rearranged cancer chromosomes from karyotype graphs}},
  doi          = {10.1186/s12859-019-3208-4},
  volume       = {20},
  year         = {2019},
}

@article{7225,
  abstract     = {This is a literature teaching resource review for biologically inspired microfluidics courses
or exploring the diverse applications of microfluidics. The structure is around key papers and model
organisms. While courses gradually change over time, a focus remains on understanding how
microfluidics has developed as well as what it can and cannot do for researchers. As a primary
starting point, we cover micro-fluid mechanics principles and microfabrication of devices. A variety
of applications are discussed using model prokaryotic and eukaryotic organisms from the set
of bacteria (Escherichia coli), trypanosomes (Trypanosoma brucei), yeast (Saccharomyces cerevisiae),
slime molds (Physarum polycephalum), worms (Caenorhabditis elegans), flies (Drosophila melangoster),
plants (Arabidopsis thaliana), and mouse immune cells (Mus musculus). Other engineering and
biochemical methods discussed include biomimetics, organ on a chip, inkjet, droplet microfluidics,
biotic games, and diagnostics. While we have not yet reached the end-all lab on a chip,
microfluidics can still be used effectively for specific applications.},
  author       = {Merrin, Jack},
  issn         = {2306-5354},
  journal      = {Bioengineering},
  number       = {4},
  publisher    = {MDPI},
  title        = {{Frontiers in microfluidics, a teaching resource review}},
  doi          = {10.3390/bioengineering6040109},
  volume       = {6},
  year         = {2019},
}

@article{7226,
  author       = {Jaksic, Vojkan and Seiringer, Robert},
  issn         = {0022-2488},
  journal      = {Journal of Mathematical Physics},
  number       = {12},
  publisher    = {AIP Publishing},
  title        = {{Introduction to the Special Collection: International Congress on Mathematical Physics (ICMP) 2018}},
  doi          = {10.1063/1.5138135},
  volume       = {60},
  year         = {2019},
}

@inproceedings{7230,
  abstract     = {Simple drawings of graphs are those in which each pair of edges share at most one point, either a common endpoint or a proper crossing. In this paper we study the problem of extending a simple drawing D(G) of a graph G by inserting a set of edges from the complement of G into D(G) such that the result is a simple drawing. In the context of rectilinear drawings, the problem is trivial. For pseudolinear drawings, the existence of such an extension follows from Levi’s enlargement lemma. In contrast, we prove that deciding if a given set of edges can be inserted into a simple drawing is NP-complete. Moreover, we show that the maximization version of the problem is APX-hard. We also present a polynomial-time algorithm for deciding whether one edge uv can be inserted into D(G) when {u,v} is a dominating set for the graph G.},
  author       = {Arroyo Guevara, Alan M and Derka, Martin and Parada, Irene},
  booktitle    = {27th International Symposium on Graph Drawing and Network Visualization},
  isbn         = {978-3-0303-5801-3},
  issn         = {1611-3349},
  location     = {Prague, Czech Republic},
  pages        = {230--243},
  publisher    = {Springer Nature},
  title        = {{Extending simple drawings}},
  doi          = {10.1007/978-3-030-35802-0_18},
  volume       = {11904},
  year         = {2019},
}

@inproceedings{7231,
  abstract     = {Piecewise Barrier Tubes (PBT) is a new technique for flowpipe overapproximation for nonlinear systems with polynomial dynamics, which leverages a combination of barrier certificates. PBT has advantages over traditional time-step based methods in dealing with those nonlinear dynamical systems in which there is a large difference in speed between trajectories, producing an overapproximation that is time independent. However, the existing approach for PBT is not efficient due to the application of interval methods for enclosure-box computation, and it can only deal with continuous dynamical systems without uncertainty. In this paper, we extend the approach with the ability to handle both continuous and hybrid dynamical systems with uncertainty that can reside in parameters and/or noise. We also improve the efficiency of the method significantly, by avoiding the use of interval-based methods for the enclosure-box computation without loosing soundness. We have developed a C++ prototype implementing the proposed approach and we evaluate it on several benchmarks. The experiments show that our approach is more efficient and precise than other methods in the literature.},
  author       = {Kong, Hui and Bartocci, Ezio and Jiang, Yu and Henzinger, Thomas A},
  booktitle    = {17th International Conference on Formal Modeling and Analysis of Timed Systems},
  isbn         = {978-3-0302-9661-2},
  issn         = {1611-3349},
  location     = {Amsterdam, The Netherlands},
  pages        = {123--141},
  publisher    = {Springer Nature},
  title        = {{Piecewise robust barrier tubes for nonlinear hybrid systems with uncertainty}},
  doi          = {10.1007/978-3-030-29662-9_8},
  volume       = {11750},
  year         = {2019},
}

@article{7275,
  abstract     = {Aprotic alkali metal–oxygen batteries require reversible formation of metal superoxide or peroxide on cycling. Severe parasitic reactions cause poor rechargeability, efficiency, and cycle life and have been shown to be caused by singlet oxygen (1O2) that forms at all stages of cycling. However, its formation mechanism remains unclear. We show that disproportionation of superoxide, the product or intermediate on discharge and charge, to peroxide and oxygen is responsible for 1O2 formation. While the overall reaction is driven by the stability of peroxide and thus favored by stronger Lewis acidic cations such as Li+, the 1O2 fraction is enhanced by weak Lewis acids such as organic cations. Concurrently, the metal peroxide yield drops with increasing 1O2. The results explain a major parasitic pathway during cell cycling and the growing severity in K–, Na–, and Li–O2 cells based on the growing propensity for disproportionation. High capacities and rates with peroxides are now realized to require solution processes, which form peroxide or release O2via disproportionation. The results therefore establish the central dilemma that disproportionation is required for high capacity but also responsible for irreversible reactions. Highly reversible cell operation requires hence finding reaction routes that avoid disproportionation.},
  author       = {Mourad, Eléonore and Petit, Yann K. and Spezia, Riccardo and Samojlov, Aleksej and Summa, Francesco F. and Prehal, Christian and Leypold, Christian and Mahne, Nika and Slugovc, Christian and Fontaine, Olivier and Brutti, Sergio and Freunberger, Stefan Alexander},
  issn         = {1754-5692},
  journal      = {Energy & Environmental Science},
  number       = {8},
  pages        = {2559--2568},
  publisher    = {RSC},
  title        = {{Singlet oxygen from cation driven superoxide disproportionation and consequences for aprotic metal–O2 batteries}},
  doi          = {10.1039/c9ee01453e},
  volume       = {12},
  year         = {2019},
}

@article{7276,
  abstract     = {Singlet oxygen (1O2) causes a major fraction of the parasitic chemistry during the cycling of non‐aqueous alkali metal‐O2 batteries and also contributes to interfacial reactivity of transition‐metal oxide intercalation compounds. We introduce DABCOnium, the mono alkylated form of 1,4‐diazabicyclo[2.2.2]octane (DABCO), as an efficient 1O2 quencher with an unusually high oxidative stability of ca. 4.2 V vs. Li/Li+. Previous quenchers are strongly Lewis basic amines with too low oxidative stability. DABCOnium is an ionic liquid, non‐volatile, highly soluble in the electrolyte, stable against superoxide and peroxide, and compatible with lithium metal. The electrochemical stability covers the required range for metal–O2 batteries and greatly reduces 1O2 related parasitic chemistry as demonstrated for the Li–O2 cell.},
  author       = {Petit, Yann K. and Leypold, Christian and Mahne, Nika and Mourad, Eléonore and Schafzahl, Lukas and Slugovc, Christian and Borisov, Sergey M. and Freunberger, Stefan Alexander},
  issn         = {1433-7851},
  journal      = {Angewandte Chemie International Edition},
  number       = {20},
  pages        = {6535--6539},
  publisher    = {Wiley},
  title        = {{DABCOnium: An efficient and high-voltage stable singlet oxygen quencher for metal-O2 cells}},
  doi          = {10.1002/anie.201901869},
  volume       = {58},
  year         = {2019},
}

@article{7280,
  abstract     = {Non-aqueous lithium-oxygen batteries cycle by forming lithium peroxide during discharge and oxidizing it during recharge. The significant problem of oxidizing the solid insulating lithium peroxide can greatly be facilitated by incorporating redox mediators that shuttle electron-holes between the porous substrate and lithium peroxide. Redox mediator stability is thus key for energy efficiency, reversibility, and cycle life. However, the gradual deactivation of redox mediators during repeated cycling has not conclusively been explained. Here, we show that organic redox mediators are predominantly decomposed by singlet oxygen that forms during cycling. Their reaction with superoxide, previously assumed to mainly trigger their degradation, peroxide, and dioxygen, is orders of magnitude slower in comparison. The reduced form of the mediator is markedly more reactive towards singlet oxygen than the oxidized form, from which we derive reaction mechanisms supported by density functional theory calculations. Redox mediators must thus be designed for stability against singlet oxygen.},
  author       = {Kwak, Won-Jin and Kim, Hun and Petit, Yann K. and Leypold, Christian and Nguyen, Trung Thien and Mahne, Nika and Redfern, Paul and Curtiss, Larry A. and Jung, Hun-Gi and Borisov, Sergey M. and Freunberger, Stefan Alexander and Sun, Yang-Kook},
  issn         = {2041-1723},
  journal      = {Nature Communications},
  publisher    = {Springer Nature},
  title        = {{Deactivation of redox mediators in lithium-oxygen batteries by singlet oxygen}},
  doi          = {10.1038/s41467-019-09399-0},
  volume       = {10},
  year         = {2019},
}

@article{7281,
  abstract     = {Li–O2 batteries are plagued by side reactions that cause poor rechargeability and efficiency. These reactions were recently revealed to be predominantly caused by singlet oxygen, which can be neutralized by chemical traps or physical quenchers. However, traps are irreversibly consumed and thus only active for a limited time, and so far identified quenchers lack oxidative stability to be suitable for typically required recharge potentials. Thus, reducing the charge potential within the stability limit of the quencher and/or finding more stable quenchers is required. Here, we show that dimethylphenazine as a redox mediator decreases the charge potential well within the stability limit of the quencher 1,4-diazabicyclo[2.2.2]octane. The quencher can thus mitigate the parasitic reactions without being oxidatively decomposed. At the same time the quencher protects the redox mediator from singlet oxygen attack. The mutual conservation of the redox mediator and the quencher is rational for stable and effective Li–O2 batteries.},
  author       = {Kwak, Won-Jin and Freunberger, Stefan Alexander and Kim, Hun and Park, Jiwon and Nguyen, Trung Thien and Jung, Hun-Gi and Byon, Hye Ryung and Sun, Yang-Kook},
  issn         = {2155-5435},
  journal      = {ACS Catalysis},
  number       = {11},
  pages        = {9914--9922},
  publisher    = {ACS},
  title        = {{Mutual conservation of redox mediator and singlet oxygen quencher in Lithium–Oxygen batteries}},
  doi          = {10.1021/acscatal.9b01337},
  volume       = {9},
  year         = {2019},
}

@article{7282,
  abstract     = {Interphases that form on the anode surface of lithium-ion batteries are critical for performance and lifetime, but are poorly understood. Now, a decade-old misconception regarding a main component of the interphase has been revealed, which could potentially lead to improved devices.},
  author       = {Freunberger, Stefan Alexander},
  issn         = {1755-4330},
  journal      = {Nature Chemistry},
  number       = {9},
  pages        = {761--763},
  publisher    = {Springer Nature},
  title        = {{Interphase identity crisis}},
  doi          = {10.1038/s41557-019-0311-0},
  volume       = {11},
  year         = {2019},
}

@article{7283,
  abstract     = {Potassium–air batteries, which suffer from oxygen cathode and potassium metal anode degradation, can be cycled thousands of times when an organic anode replaces the metal.},
  author       = {Petit, Yann K. and Freunberger, Stefan Alexander},
  issn         = {1476-1122},
  journal      = {Nature Materials},
  number       = {4},
  pages        = {301--302},
  publisher    = {Springer Nature},
  title        = {{Thousands of cycles}},
  doi          = {10.1038/s41563-019-0313-8},
  volume       = {18},
  year         = {2019},
}

@article{7284,
  abstract     = {In this issue of Joule, Dongmin Im and coworkers from Samsung in South Korea describe a prototype lithium-O2 battery that reaches ∼700 Wh kg–1 and ∼600 Wh L–1 on the cell level. They cut all components to the minimum to reach this value. Difficulties filling the pores with discharge product and inhomogeneous cell utilization turn out to limit the achievable energy. Their work underlines the importance of reporting performance with respect to full cell weight and volume.},
  author       = {Prehal, Christian and Freunberger, Stefan Alexander},
  issn         = {2542-4351},
  journal      = {Joule},
  number       = {2},
  pages        = {321--323},
  publisher    = {Elsevier},
  title        = {{Li-O2 cell-scale energy densities}},
  doi          = {10.1016/j.joule.2019.01.020},
  volume       = {3},
  year         = {2019},
}

@article{73,
  abstract     = {We consider the space of probability measures on a discrete set X, endowed with a dynamical optimal transport metric. Given two probability measures supported in a subset Y⊆X, it is natural to ask whether they can be connected by a constant speed geodesic with support in Y at all times. Our main result answers this question affirmatively, under a suitable geometric condition on Y introduced in this paper. The proof relies on an extension result for subsolutions to discrete Hamilton-Jacobi equations, which is of independent interest.},
  author       = {Erbar, Matthias and Maas, Jan and Wirth, Melchior},
  issn         = {0944-2669},
  journal      = {Calculus of Variations and Partial Differential Equations},
  number       = {1},
  publisher    = {Springer},
  title        = {{On the geometry of geodesics in discrete optimal transport}},
  doi          = {10.1007/s00526-018-1456-1},
  volume       = {58},
  year         = {2019},
}

@article{7340,
  abstract     = {Coupling of endoplasmic reticulum stress to dimerisation‑dependent activation of the UPR transducer IRE1 is incompletely understood. Whilst the luminal co-chaperone ERdj4 promotes a complex between the Hsp70 BiP and IRE1's stress-sensing luminal domain (IRE1LD) that favours the latter's monomeric inactive state and loss of ERdj4 de-represses IRE1, evidence linking these cellular and in vitro observations is presently lacking. We report that enforced loading of endogenous BiP onto endogenous IRE1α repressed UPR signalling in CHO cells and deletions in the IRE1α locus that de-repressed the UPR in cells, encode flexible regions of IRE1LD that mediated BiP‑induced monomerisation in vitro. Changes in the hydrogen exchange mass spectrometry profile of IRE1LD induced by ERdj4 and BiP confirmed monomerisation and were consistent with active destabilisation of the IRE1LD dimer. Together, these observations support a competition model whereby waning ER stress passively partitions ERdj4 and BiP to IRE1LD to initiate active repression of UPR signalling.},
  author       = {Amin-Wetzel, Niko Paresh and Neidhardt, Lisa and Yan, Yahui and Mayer, Matthias P. and Ron, David},
  issn         = {2050-084X},
  journal      = {eLife},
  publisher    = {eLife Sciences Publications},
  title        = {{Unstructured regions in IRE1α specify BiP-mediated destabilisation of the luminal domain dimer and repression of the UPR}},
  doi          = {10.7554/eLife.50793},
  volume       = {8},
  year         = {2019},
}

@unpublished{7358,
  abstract     = {Telencephalic organoids generated from human pluripotent stem cells (hPSCs) are emerging as an effective system to study the distinct features of the developing human brain and the underlying causes of many neurological disorders. While progress in organoid technology has been steadily advancing, many challenges remain including rampant batch-to-batch and cell line-to-cell line variability and irreproducibility. Here, we demonstrate that a major contributor to successful cortical organoid production is the manner in which hPSCs are maintained prior to differentiation. Optimal results were achieved using fibroblast-feeder-supported hPSCs compared to feeder-independent cells, related to differences in their transcriptomic states. Feeder-supported hPSCs display elevated activation of diverse TGFβ superfamily signaling pathways and increased expression of genes associated with naïve pluripotency. We further identify combinations of TGFβ-related growth factors that are necessary and together sufficient to impart broad telencephalic organoid competency to feeder-free hPSCs and enable reproducible formation of brain structures suitable for disease modeling.},
  author       = {Watanabe, Momoko and Haney, Jillian R. and Vishlaghi, Neda and Turcios, Felix and Buth, Jessie E. and Gu, Wen and Collier, Amanda J. and Miranda, Osvaldo and Chen, Di and Sabri, Shan and Clark, Amander T. and Plath, Kathrin and Christofk, Heather R. and Gandal, Michael J. and Novitch, Bennett G.},
  booktitle    = {bioRxiv},
  pages        = {75},
  publisher    = {Cold Spring Harbor Laboratory},
  title        = {{TGFβ superfamily signaling regulates the state of human stem cell pluripotency and competency to create telencephalic organoids}},
  doi          = {10.1101/2019.12.13.875773},
  year         = {2019},
}

@article{7393,
  abstract     = {The study of parallel ecological divergence provides important clues to the operation of natural selection. Parallel divergence often occurs in heterogeneous environments with different kinds of environmental gradients in different locations, but the genomic basis underlying this process is unknown. We investigated the genomics of rapid parallel adaptation in the marine snail Littorina saxatilis in response to two independent environmental axes (crab-predation versus wave-action and low-shore versus high-shore). Using pooled whole-genome resequencing, we show that sharing of genomic regions of high differentiation between environments is generally low but increases at smaller spatial scales. We identify different shared genomic regions of divergence for each environmental axis and show that most of these regions overlap with candidate chromosomal inversions. Several inversion regions are divergent and polymorphic across many localities. We argue that chromosomal inversions could store shared variation that fuels rapid parallel adaptation to heterogeneous environments, possibly as balanced polymorphism shared by adaptive gene flow.},
  author       = {Morales, Hernán E. and Faria, Rui and Johannesson, Kerstin and Larsson, Tomas and Panova, Marina and Westram, Anja M and Butlin, Roger K.},
  issn         = {2375-2548},
  journal      = {Science Advances},
  number       = {12},
  publisher    = {AAAS},
  title        = {{Genomic architecture of parallel ecological divergence: Beyond a single environmental contrast}},
  doi          = {10.1126/sciadv.aav9963},
  volume       = {5},
  year         = {2019},
}

@article{7395,
  abstract     = {The mitochondrial electron transport chain complexes are organized into supercomplexes (SCs) of defined stoichiometry, which have been proposed to regulate electron flux via substrate channeling. We demonstrate that CoQ trapping in the isolated SC I+III2 limits complex (C)I turnover, arguing against channeling. The SC structure, resolved at up to 3.8 Å in four distinct states, suggests that CoQ oxidation may be rate limiting because of unequal access of CoQ to the active sites of CIII2. CI shows a transition between “closed” and “open” conformations, accompanied by the striking rotation of a key transmembrane helix. Furthermore, the state of CI affects the conformational flexibility within CIII2, demonstrating crosstalk between the enzymes. CoQ was identified at only three of the four binding sites in CIII2, suggesting that interaction with CI disrupts CIII2 symmetry in a functionally relevant manner. Together, these observations indicate a more nuanced functional role for the SCs.},
  author       = {Letts, James A and Fiedorczuk, Karol and Degliesposti, Gianluca and Skehel, Mark and Sazanov, Leonid A},
  issn         = {1097-2765},
  journal      = {Molecular Cell},
  number       = {6},
  pages        = {1131--1146.e6},
  publisher    = {Cell Press},
  title        = {{Structures of respiratory supercomplex I+III2 reveal functional and conformational crosstalk}},
  doi          = {10.1016/j.molcel.2019.07.022},
  volume       = {75},
  year         = {2019},
}

@article{7396,
  abstract     = {The angular momentum of molecules, or, equivalently, their rotation in three-dimensional space, is ideally suited for quantum control. Molecular angular momentum is naturally quantized, time evolution is governed by a well-known Hamiltonian with only a few accurately known parameters, and transitions between rotational levels can be driven by external fields from various parts of the electromagnetic spectrum. Control over the rotational motion can be exerted in one-, two-, and many-body scenarios, thereby allowing one to probe Anderson localization, target stereoselectivity of bimolecular reactions, or encode quantum information to name just a few examples. The corresponding approaches to quantum control are pursued within separate, and typically disjoint, subfields of physics, including ultrafast science, cold collisions, ultracold gases, quantum information science, and condensed-matter physics. It is the purpose of this review to present the various control phenomena, which all rely on the same underlying physics, within a unified framework. To this end, recall the Hamiltonian for free rotations, assuming the rigid rotor approximation to be valid, and summarize the different ways for a rotor to interact with external electromagnetic fields. These interactions can be exploited for control—from achieving alignment, orientation, or laser cooling in a one-body framework, steering bimolecular collisions, or realizing a quantum computer or quantum simulator in the many-body setting.},
  author       = {Koch, Christiane P. and Lemeshko, Mikhail and Sugny, Dominique},
  issn         = {1539-0756},
  journal      = {Reviews of Modern Physics},
  number       = {3},
  publisher    = {American Physical Society},
  title        = {{Quantum control of molecular rotation}},
  doi          = {10.1103/revmodphys.91.035005},
  volume       = {91},
  year         = {2019},
}

@article{7397,
  abstract     = {Polymer additives can substantially reduce the drag of turbulent flows and the upperlimit, the so called “maximum drag reduction” (MDR) asymptote is universal, i.e. inde-pendent of the type of polymer and solvent used. Until recently, the consensus was that,in this limit, flows are in a marginal state where only a minimal level of turbulence activ-ity persists. Observations in direct numerical simulations using minimal sized channelsappeared  to  support  this  view  and  reported  long  “hibernation”  periods  where  turbu-lence is marginalized. In simulations of pipe flow we find that, indeed, with increasingWeissenberg number (Wi), turbulence expresses long periods of hibernation if the domainsize is small. However, with increasing pipe length, the temporal hibernation continuouslyalters to spatio-temporal intermittency and here the flow consists of turbulent puffs sur-rounded by laminar flow. Moreover, upon an increase in Wi, the flow fully relaminarises,in agreement with recent experiments. At even larger Wi, a different instability is en-countered causing a drag increase towards MDR. Our findings hence link earlier minimalflow unit simulations with recent experiments and confirm that the addition of polymersinitially suppresses Newtonian turbulence and leads to a reverse transition. The MDRstate on the other hand results from a separate instability and the underlying dynamicscorresponds to the recently proposed state of elasto-inertial-turbulence (EIT).},
  author       = {Lopez Alonso, Jose M and Choueiri, George H and Hof, Björn},
  issn         = {1469-7645},
  journal      = {Journal of Fluid Mechanics},
  pages        = {699--719},
  publisher    = {Cambridge University Press},
  title        = {{Dynamics of viscoelastic pipe flow at low Reynolds numbers in the maximum drag reduction limit}},
  doi          = {10.1017/jfm.2019.486},
  volume       = {874},
  year         = {2019},
}

