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  1. ...along the northeast coast. (F) Branch not belonging to the primary European branch in Figure 2A, corresponding to the Iberian Peninsula and Morocco. Population structure extends on a north–south axis from Africa to Europe over the Strait of Gibraltar. (G) Branch corresponding to Morocco, showing fine...
  2. ...recombination map for a rhesus macaque pedigree using crossovers among 241 microsatellite loci (Rogers et al. 2006) also suggested reduced recombination per megabase in rhesus relative to human. Demographic analysis of two rhesus macaque populations The estimated effective population sizes, based on the number...
  3. .... Abstract Genetic and fossil evidence supports a single, recent (<200,000 yr) origin of modern Homo sapiens in Africa, followed by later population divergence and dispersal across the globe (the “Out of Africa” model). However, there is less agreement on the exact nature of this migration event...
  4. ...clustering, and the corresponding nodes give the number of populations identified at that stage. For visualization, see Figure 3. Additionally, tangleGen offers a pruning option that allows to exclude the external branches in the tangles tree, which are not supported by a sufficient number of cuts...
  5. ...branches, and how they relate to the population genetics of Africa over a time horizon that begins well before the exit from the continent. Results A high-depth resequencing (average 503) of ;1.5 Mb of the MSY was performed in 68 unrelated males representing major Y chromosome haplogroups (Supplemental...
  6. ...populations from Madagascar and South Africa diverged around 200 kya, the two S. dumicola populations in North and South Namibia diverged 20 kya, and the two S. sarasinorum populations from Himalaya and Sri Lanka diverged ∼110 kya.The pseudodiploid of social species collapsed two heavily inbred diploid...
  7. ...expansion factor inferred by Nelson et al. (2012) in the CEU subpopulation. The ancestral population bottlenecks reflect the out-of-Africa bottleneck and the European-Asian population split, and these parameters were set to those estimated by Keinan et al. (2007). The population size functions...
  8. ...and recombination. J Hered 101: S21–S33. doi:10.1093/jhered/esq009 ↵Asher JH. 1970. Parthenogenesis and genetic variability. II. One-locus models for various diploid populations. Genetics 66: 369–391. doi:10.1093/genetics/66.2.369 ↵Blouin M, Parsons M, Lacaille V, Lotz S. 1996. Use of microsatellite loci...
  9. ..., as restriction fragment length polymorphisms, microsatellites, and small-scale DNA sequencing (e.g., Kreitman 1983) broadened the range of questions open to empirical investigation. With the recent flood of -wide single nucleotide polymorphism (SNP) data, and now the advent of fully sequenced population samples...
  10. ...location of the source population. Patterns of microsatellite and haplotype diversity in theHumanGenomeDiversity Project (HGDP) panel fit this expectation, with the strongest negative correlation being observed between diversity and distance from sub-Saharan Africa (Ramachandran et al. 2005; Li et al. 2008...
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