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    <titleInfo>
      <title>Revisiting F-IS, F-ST, Wahlund effects, and Null alleles</title>
    </titleInfo>
    <name type="personnal">
      <namePart type="family">De Meeûs</namePart>
      <namePart type="given">Thierry</namePart>
      <role>
        <roleTerm type="text">auteur</roleTerm>
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      <affiliation>IRD</affiliation>
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      <languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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    <abstract>Null alleles and Wahlund effects are well known causes of heterozygote deficits in empirical population genetics studies as compared to Hardy-Weinberg genotypic expectations. Some authors have theoretically studied the relationship of Wright's F-IS computed from subsamples displaying a Wahlund effect and F-ST before the Wahlund effect, as can occasionally be obtained from populations of long-lived organisms. In the 2 subsample case, a positive relationship between these 2 parameters across loci would represent a signature of Wahlund effects. Nevertheless, for most organisms, getting 2 independent subsamples of the same cohort and population, one with a Wahlund effect and the other without, is almost never achieved and most of the time, empirical population geneticists only collect a single sample, with or without a Wahlund effect, or with or without null alleles. Another issue is that null allele increase F-IS and F-ST altogether and thus may also create such correlation. In this article, I show that, for organisms collected in a single sample, which corresponds to the most common situation, Wahlund effects and null alleles affect the values of both F-Is and F-ST though in the opposite direction. I also show that Wahlund effect produces no or weak positive correlation between the 2 F-statisties, while null alleles generate a strong positive correlation between them. Variation of these F-statistics is small and even minimized for F-ST under Wahlund effects as compared to null alleles. I finally propose a determination key to interpret data with heterozygote deficits.</abstract>
    <targetAudience authority="marctarget">specialized</targetAudience>
    <subject>
      <topic>differentiation</topic>
      <topic>F-statistics</topic>
      <topic>genetic identities</topic>
      <topic>inbreeding</topic>
    </subject>
    <classification authority="local">020</classification>
    <relatedItem type="host">
      <titleInfo>
        <title>Journal of Heredity</title>
      </titleInfo>
      <part>
        <detail type="volume">
          <number>109</number>
        </detail>
        <detail type="volume">
          <number>4</number>
        </detail>
        <extent unit="pages">
          <list> 446-456</list>
        </extent>
      </part>
      <originInfo>
        <dateIssued>2018</dateIssued>
      </originInfo>
      <identifier type="issn">0022-1503</identifier>
    </relatedItem>
    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010073032</identifier>
    <identifier type="doi">10.1093/jhered/esx106</identifier>
    <identifier type="issn">0022-1503</identifier>
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      <shelfLocator>[F B010073032]</shelfLocator>
      <url usage="primary display" access="object in context">https://www.documentation.ird.fr/hor/fdi:010073032</url>
      <url access="row object">https://www.documentation.ird.fr/intranet/publi/2018/06/010073032.pdf</url>
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    <accessCondition type="restriction access" displayLabel="Accès réservé">Accès réservé (Intranet de l'IRD)</accessCondition>
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      <recordCreationDate encoding="w3cdtf">2018-07-03</recordCreationDate>
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