<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>Kousathanas, Athanasios</dc:creator>
  <dc:creator>Leuenberger, Christoph</dc:creator>
  <dc:creator>Link, Vivian</dc:creator>
  <dc:creator>Sell, Christian</dc:creator>
  <dc:creator>Burger, Joachim</dc:creator>
  <dc:creator>Wegmann, Daniel</dc:creator>
  <dc:date>2017-01-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">While genetic diversity can be quantified accurately from high coverage sequencing  data, it is often desirable to obtain such estimates from data with low coverage, either  to save costs or because of low DNA quality, as is observed for ancient samples.  Here, we introduce a method to accurately infer heterozygosity probabilistically from  sequences with average coverage Embedded Image of a single individual. The method  relaxes the infinite sites assumption of previous methods, does not require a reference  sequence, except for the initial alignment of the sequencing data, and takes into  account both variable sequencing errors and potential postmortem damage. It is thus  also applicable to nonmodel organisms and ancient genomes. Since error rates as  reported by sequencing machines are generally distorted and require recalibration, we  also introduce a method to accurately infer recalibration parameters in the presence of  postmortem damage. This method does not require knowledge about the underlying  genome sequence, but instead works with haploid data (e.g., from the X-chromosome  from mammalian males) and integrates over the unknown genotypes. Using extensive  simulations we show that a few megabasepairs of haploid data are sufficient for  accurate recalibration, even at average coverages as low as Embedded Image At  similar coverages, our method also produces very accurate estimates of  heterozygosity down to Embedded Image within windows of about 1 Mbp. We further  illustrate the usefulness of our approach by inferring genome-wide patterns of diversity  for several ancient human samples, and we found that 3000–5000-year-old samples  showed diversity patterns comparable to those of modern humans. In contrast, two  European hunter-gatherer samples exhibited not only considerably lower levels of  diversity than modern samples, but also highly distinct distributions of diversity along  their genomes. Interestingly, these distributions were also very different between the  two samples, supporting earlier conclusions of a highly diverse and structured  population in Europe prior to the arrival of farming.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/305403</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305403/files/weg_iha_sm.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305403/files/weg_iha.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1534/genetics.116.189985</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Genetics. - 2017, vol. 205, no. 1, p. 317–332</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Inferring heterozygosity from ancient and low coverage genomes</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
