<?xml version="1.0" encoding="UTF-8"?>
<collection xmlns="http://www.loc.gov/MARC21/slim">
 <record>
  <leader>     caa a22        4500</leader>
  <controlfield tag="001">397573537</controlfield>
  <controlfield tag="003">CHVBK</controlfield>
  <controlfield tag="005">20180308164848.0</controlfield>
  <controlfield tag="007">cr unu---uuuuu</controlfield>
  <controlfield tag="008">161202e199611  xx      s     000 0 eng  </controlfield>
  <datafield tag="024" ind1="7" ind2="0">
   <subfield code="a">10.1093/hmg/5.11.1759</subfield>
   <subfield code="2">doi</subfield>
  </datafield>
  <datafield tag="035" ind1=" " ind2=" ">
   <subfield code="a">(NATIONALLICENCE)oxford-10.1093/hmg/5.11.1759</subfield>
  </datafield>
  <datafield tag="245" ind1="0" ind2="0">
   <subfield code="a">Network Analysis of Human Y Microsatellite Haplotypes</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Gillian Cooper, William Amos, Dorota Hoffman, David C. Rubinsztein]</subfield>
  </datafield>
  <datafield tag="520" ind1="3" ind2=" ">
   <subfield code="a">To investigate the utility of Y chromosome micro-satellites for studying human male-lineage evolution, we typed samples from three populations for five tetranucleotide repeats and an Alu insertion polymorphism. We found very high levels of haplotype diversity and evidence that most mutations involve the gain or loss of only one repeat unit, implying that any given microsatellite haplotype may have arisen independently on two or more Y-chromosome lineages. Together, these factors suggest that interpretation of small sample sizes (&lt;30) will be problematic. By typing a large sample of individuals (n = 174) from one population, East Anglia, we were able to construct a haplotype network. The network exhibits a well-connected core structure of commoner haplotypes. Computer simulations based on this network estimate the convergence time for African and Caucasian groups may be between 1.4 and 1.8 times as long as the convergence of the East Anglian population. Based on our comparison between large and small sample sizes, we suggest that large sample sizes are necessary in order to interpret Y-microsatellite haplotypes, and that a network analysis of the type we describe may prove informative in future studies.</subfield>
  </datafield>
  <datafield tag="540" ind1=" " ind2=" ">
   <subfield code="a">© 1996 Oxford University Press</subfield>
  </datafield>
  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Cooper</subfield>
   <subfield code="D">Gillian</subfield>
   <subfield code="u">University of Cambridge, Department of Genetics, Downing Street, Cambridge CB2 3EH, UK</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Amos</subfield>
   <subfield code="D">William</subfield>
   <subfield code="u">University of Cambridge, Department of Genetics, Downing Street, Cambridge CB2 3EH, UK</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Hoffman</subfield>
   <subfield code="D">Dorota</subfield>
   <subfield code="u">East Anglian Regional Genetics Service Molecular Genetics Laboratory Department of Clinical Genetics, Box 158, Addenbrooke's NHS Trust, Hills Road, Cambridge CB2 2QQ, UK</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Rubinsztein</subfield>
   <subfield code="D">David C.</subfield>
   <subfield code="u">East Anglian Regional Genetics Service Molecular Genetics Laboratory Department of Clinical Genetics, Box 158, Addenbrooke's NHS Trust, Hills Road, Cambridge CB2 2QQ, UK</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="773" ind1="0" ind2=" ">
   <subfield code="t">Human Molecular Genetics</subfield>
   <subfield code="d">Oxford University Press</subfield>
   <subfield code="g">5/11(1996-11), 1759-1766</subfield>
   <subfield code="x">0964-6906</subfield>
   <subfield code="q">5:11&lt;1759</subfield>
   <subfield code="1">1996</subfield>
   <subfield code="2">5</subfield>
   <subfield code="o">hmg</subfield>
  </datafield>
  <datafield tag="856" ind1="4" ind2="0">
   <subfield code="u">https://doi.org/10.1093/hmg/5.11.1759</subfield>
   <subfield code="q">text/html</subfield>
   <subfield code="z">Onlinezugriff via DOI</subfield>
  </datafield>
  <datafield tag="908" ind1=" " ind2=" ">
   <subfield code="D">1</subfield>
   <subfield code="a">research-article</subfield>
   <subfield code="2">jats</subfield>
  </datafield>
  <datafield tag="950" ind1=" " ind2=" ">
   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="P">856</subfield>
   <subfield code="E">40</subfield>
   <subfield code="u">https://doi.org/10.1093/hmg/5.11.1759</subfield>
   <subfield code="q">text/html</subfield>
   <subfield code="z">Onlinezugriff via DOI</subfield>
  </datafield>
  <datafield tag="950" ind1=" " ind2=" ">
   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="P">700</subfield>
   <subfield code="E">1-</subfield>
   <subfield code="a">Cooper</subfield>
   <subfield code="D">Gillian</subfield>
   <subfield code="u">University of Cambridge, Department of Genetics, Downing Street, Cambridge CB2 3EH, UK</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="950" ind1=" " ind2=" ">
   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="P">700</subfield>
   <subfield code="E">1-</subfield>
   <subfield code="a">Amos</subfield>
   <subfield code="D">William</subfield>
   <subfield code="u">University of Cambridge, Department of Genetics, Downing Street, Cambridge CB2 3EH, UK</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="950" ind1=" " ind2=" ">
   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="P">700</subfield>
   <subfield code="E">1-</subfield>
   <subfield code="a">Hoffman</subfield>
   <subfield code="D">Dorota</subfield>
   <subfield code="u">East Anglian Regional Genetics Service Molecular Genetics Laboratory Department of Clinical Genetics, Box 158, Addenbrooke's NHS Trust, Hills Road, Cambridge CB2 2QQ, UK</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="950" ind1=" " ind2=" ">
   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="P">700</subfield>
   <subfield code="E">1-</subfield>
   <subfield code="a">Rubinsztein</subfield>
   <subfield code="D">David C.</subfield>
   <subfield code="u">East Anglian Regional Genetics Service Molecular Genetics Laboratory Department of Clinical Genetics, Box 158, Addenbrooke's NHS Trust, Hills Road, Cambridge CB2 2QQ, UK</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="950" ind1=" " ind2=" ">
   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="P">773</subfield>
   <subfield code="E">0-</subfield>
   <subfield code="t">Human Molecular Genetics</subfield>
   <subfield code="d">Oxford University Press</subfield>
   <subfield code="g">5/11(1996-11), 1759-1766</subfield>
   <subfield code="x">0964-6906</subfield>
   <subfield code="q">5:11&lt;1759</subfield>
   <subfield code="1">1996</subfield>
   <subfield code="2">5</subfield>
   <subfield code="o">hmg</subfield>
  </datafield>
  <datafield tag="900" ind1=" " ind2="7">
   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">CC BY-NC-4.0</subfield>
   <subfield code="u">http://creativecommons.org/licenses/by-nc/4.0</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="898" ind1=" " ind2=" ">
   <subfield code="a">BK010053</subfield>
   <subfield code="b">XK010053</subfield>
   <subfield code="c">XK010000</subfield>
  </datafield>
  <datafield tag="949" ind1=" " ind2=" ">
   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="F">NATIONALLICENCE</subfield>
   <subfield code="b">NL-oxford</subfield>
  </datafield>
 </record>
</collection>
