<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Ferrer-Admetlla, Anna</dc:creator>
  <dc:creator>Leuenberger, Christoph</dc:creator>
  <dc:creator>Jensen, Jeffrey D.</dc:creator>
  <dc:creator>Wegmann, Daniel</dc:creator>
  <dc:date>2016-01-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The joint and accurate inference of selection and demography from genetic data is  considered a particularly challenging question in population genetics, since both  process may lead to very similar patterns of genetic diversity. However, additional  information for disentangling these effects may be obtained by observing changes in  allele frequencies over multiple time points. Such data is common in experimental  evolution studies, as well as in the comparison of ancient and contemporary samples.  Leveraging this information, however, has been computationally challenging,  particularly when considering multi-locus data sets. To overcome these issues, we  introduce a novel, discrete approximation for diffusion processes, termed mean  transition time approximation, which preserves the long-term behavior of the underlying  continuous diffusion process. We then derive this approximation for the particular case  of inferring selection and demography from time series data under the classic Wright- Fisher model and demonstrate that our approximation is well suited to describe allele  trajectories through time, even when only a few states are used. We then develop a  Bayesian inference approach to jointly infer the population size and locus-specific  selection coefficients with high accuracy, and further extend this model to also infer the  rates of sequencing errors and mutations. We finally apply our approach to recent  experimental data on the evolution of drug resistance in Influenza virus, identifying  likely targets of selection and finding evidence for much larger viral population sizes  than previously reported.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/304908</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/304908/files/weg_amm.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/304908/files/weg_amm_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1534/genetics.115.184598</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Genetics. - 2016, vol. 203, no. 2, p. 831-846</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">An approximate Markov model for the wright-fisher diffusion and its application to time series data</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
