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    <title>Kersbergen, P.</title>
    <link>http://repub.eur.nl/res/aut/12438/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
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    <item>
      <title>Proportioning whole-genome single-nucleotide-polymorphism diversity for the identification of geographic population structure and genetic ancestry (Article)</title>
      <link>http://repub.eur.nl/res/pub/8485/</link>
      <pubDate>2006-01-01T00:00:00Z</pubDate>
      <description>The identification of geographic population structure and genetic ancestry
      on the basis of a minimal set of genetic markers is desirable for a wide
      range of applications in medical and forensic sciences. However, the
      absence of sharp discontinuities in the neutral genetic diversity among
      human populations implies that, in practice, a large number of neutral
      markers will be required to identify the genetic ancestry of one
      individual. We showed that it is possible to reduce the amount of markers
      required for detecting continental population structure to only 10
      single-nucleotide polymorphisms (SNPs), by applying a newly developed
      ascertainment algorithm to Affymetrix GeneChip Mapping 10K SNP array data
      that we obtained from samples of globally dispersed human individuals (the
      Y Chromosome Consortium panel). Furthermore, this set of SNPs was able to
      recover the genetic ancestry of individuals from all four continents
      represented in the original data set when applied to an independent, much
      larger, worldwide population data set (Centre d'Etude du Polymorphisme
      Humain-Human Genome Diversity Project Cell Line Panel). Finally, we
      provide evidence that the unusual patterns of genetic variation we
      observed at the respective genomic regions surrounding the five most
      informative SNPs is in agreement with local positive selection being the
      explanation for the striking SNP allele-frequency differences we found
      between continental groups of human populations.</description>
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