8c2f7318d8d821de9b2a25750586a94ab5e8c1bb lrnassar Fri Nov 15 18:50:19 2024 -0800 Giving the UI link cronjob some love by fixing all the 301 redirects. These are the bulk of the items listed on the cron. No RM. diff --git src/hg/makeDb/trackDb/human/hgdpHzy.html src/hg/makeDb/trackDb/human/hgdpHzy.html index 64385f2..309d989 100644 --- src/hg/makeDb/trackDb/human/hgdpHzy.html +++ src/hg/makeDb/trackDb/human/hgdpHzy.html @@ -1,65 +1,65 @@ <H2>Description</H2> <P> This track shows a 3-SNP moving average of <em>p(1-p)</em> where <em>p</em> is the major allele frequency (i.e. half of the expected heterozygosity) on seven continents, from SNPs genotyped in 53 populations worldwide by the -<A HREF="http://www.stanford.edu/group/morrinst/hgdp.html" TARGET=_BLANK>Human +<A HREF="https://web.stanford.edu/group/morrinst/hgdp.html" TARGET=_BLANK>Human Genome Diversity Project</A> in collaboration with the <A HREF="https://cephb.fr/en/cephdb/" TARGET=_BLANK>Centre d'Etude du Polymorphisme Humain</A> (HGDP-CEPH). This track and several others are available from the <A HREF="http://hgdp.uchicago.edu/" TARGET=_BLANK>HGDP Selection Browser</A>. </P> <H2>Methods</H2> <P> Samples collected by the HGDP-CEPH from 1,043 individuals from around the world were genotyped for 657,000 SNPs at <A HREF="https://hagsc.org/hgdp/" TARGET=_BLANK>Stanford</A>. The 53 populations were divided into seven continental groups: Africa, Middle East, Europe, South Asia, East Asia, Oceania and the Americas. Allele frequencies were used to calculate <em>p(1-p)</em> for each SNP, and then a 3-SNP average was computed for each SNP and its two neighboring SNPs.</P> <P> The associated analysis tracks HGDP FST, HGP iHS, and HGDP XP-EHH (Pickrell <em>et al.</em>) did not make use of all African populations, but instead used only the Bantu populations because a more closely related group was desired for comparison with other continental groups. For this track, separate subtracks show the expected heterozygosity of all African populations and of only Bantu populations. </P> <H2>Credits</H2> <P> Thanks to the HGDP-CEPH and Joe Pickrell in the <A HREF="http://web.stanford.edu/group/pritchardlab/home.html"TARGET=_BLANK>Pritchard lab</A> at the University of Chicago for providing these data. </P> <H2>References</H2> <P> Pickrell JK, Coop G, Novembre J, Kudaravalli S, Li J, Absher D, Srinivasan BS, Barsh GS, Myers RM, Feldman MW, Pritchard JK. <A HREF="https://www.ncbi.nlm.nih.gov/pubmed/19307593?dopt=Abstract" TARGET=_BLANK>Signals of recent positive selection in a worldwide sample of human populations</A>. <em>Genome Res.</em> 2009 May;19(5):826-37.</P> <P> Li JZ, Absher DM, Tang H, Southwick AM, Casto AM, Ramachandran S, Cann HM, Barsh GS, Feldman M, Cavalli-Sforza LL, Myers RM. <A HREF="https://www.ncbi.nlm.nih.gov/pubmed/18292342?dopt=Abstract" TARGET=_BLANK>Worldwide human relationships inferred from genome-wide patterns of variation</A>. <em>Science</em>. 2008 Feb 22;319(5866):1100-4.</P> <P> Cann HM, de Toma C, Cazes L, Legrand MF, Morel V, Piouffre L, Bodmer J, Bodmer WF, Bonne-Tamir B, Cambon-Thomsen A <em>et al.</em> <A HREF="https://www.ncbi.nlm.nih.gov/pubmed/11954565?dopt=Abstract" TARGET=_BLANK>A human genome diversity cell line panel</A>. <em>Science</em>. 2002 Apr 12;296(5566):261-2.</P>