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   	<dc:title>The genetic basis of complex traits studied via analysis of evolve and resequence experiments</dc:title>
   	<dc:title>ISTA Thesis</dc:title>
   	<dc:creator>Belohlavy, Stefanie ; https://orcid.org/0000-0002-9849-498X</dc:creator>
   	<dc:subject>ddc:576</dc:subject>
   	<dc:description>In evolve and resequence experiments, a population is sequenced, subjected to selection and
then sequenced again, so that genetic changes before and after selection can be observed at
the genetic level. Here, I use these studies to better understand the genetic basis of complex
traits - traits which depend on more than a few genes.
In the first chapter, I discuss the first evolve and resequence experiment, in which a population
of mice, the so-called &quot;Longshanks&quot; mice, were selected for tibia length while their body mass
was kept constant. The full pedigree is known. We observed a selection response on all
chromosomes and used the infinitesimal model with linkage, a model which assumes an infinite
number of genes with infinitesimally small effect sizes, as a null model. Results implied a very
polygenic basis with a few loci of major effect standing out and changing in parallel. There
was large variability between the different chromosomes in this study, probably due to LD.
In chapter two, I go on to discuss the impact of LD, on the variability in an allele-frequency
based summary statistic, giving an equation based on the initial allele frequencies, average
pairwise LD, and the first four moments of the haplotype block copy number distribution. I
describe this distribution by referring back to the founder generation. I then demonstrate
how to infer selection via a maximum likelihood scheme on the example of a single locus and
discuss how to extend this to more realistic scenarios.
In chapter three, I discuss the second evolve and resequence experiment, in which a small
population of Drosophila melanogaster was selected for increased pupal case size over 6
generations. The experiment was highly replicated with 27 lines selected within family and a
known pedigree. We observed a phenotypic selection response of over one standard deviation.
I describe the patterns in allele frequency data, including allele frequency changes and patterns
of heterozygosity, and give ideas for future work.</dc:description>
   	<dc:publisher>Institute of Science and Technology Austria</dc:publisher>
   	<dc:date>2022</dc:date>
   	<dc:type>info:eu-repo/semantics/doctoralThesis</dc:type>
   	<dc:type>doc-type:doctoralThesis</dc:type>
   	<dc:type>text</dc:type>
   	<dc:type>http://purl.org/coar/resource_type/c_db06</dc:type>
   	<dc:identifier>https://research-explorer.ista.ac.at/record/11388</dc:identifier>
   	<dc:identifier>https://research-explorer.ista.ac.at/download/11388/11398</dc:identifier>
   	<dc:source>Belohlavy S. The genetic basis of complex traits studied via analysis of evolve and resequence experiments. 2022. doi:&lt;a href=&quot;https://doi.org/10.15479/at:ista:11388&quot;&gt;10.15479/at:ista:11388&lt;/a&gt;</dc:source>
   	<dc:language>eng</dc:language>
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   	<dc:relation>info:eu-repo/semantics/altIdentifier/isbn/978-3-99078-018-3</dc:relation>
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