2010
DOI: 10.1126/science.329.5998.1467-b
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Archaeology Augments Tibet's Genetic History—Response

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Cited by 11 publications
(11 citation statements)
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“…Most current methods for conducting population genetic analysis are based on allele frequencies (reviewed in Nielsen, 2005) or a summary of allele frequencies (e.g., Gutenkunst et al, 2009; but see Yi et al, 2010), and, broadly speaking, two statistical approaches have been proposed to estimate this information from NGS data. The first approach entails calling genotypes of each individual using either a Bayesian or Likelihood framework (Hoberman et al, 2009; Li et al, 2009b; Bansal et al, 2010; DePristo et al, 2011).…”
Section: Introductionmentioning
confidence: 99%
See 2 more Smart Citations
“…Most current methods for conducting population genetic analysis are based on allele frequencies (reviewed in Nielsen, 2005) or a summary of allele frequencies (e.g., Gutenkunst et al, 2009; but see Yi et al, 2010), and, broadly speaking, two statistical approaches have been proposed to estimate this information from NGS data. The first approach entails calling genotypes of each individual using either a Bayesian or Likelihood framework (Hoberman et al, 2009; Li et al, 2009b; Bansal et al, 2010; DePristo et al, 2011).…”
Section: Introductionmentioning
confidence: 99%
“…The other approach attempts to estimate allele frequencies directly from the data without first inferring individual genotypes (Lynch, 2009; Kim et al, 2010, 2011; Martin et al, 2010). In some cases, a posterior probability is generated that provides a quantification of the uncertainty of each genotype call (e.g., Martin et al, 2010; DePristo et al, 2011) that could be directly incorporated into population genetic analyses (e.g., Yi et al, 2010). However, until population genetic analyses are further adapted to incorporate posterior probabilities, standard population genetic analyses must be applied directly to genotype calls.…”
Section: Introductionmentioning
confidence: 99%
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“…To minimize the effect of low-coverage sequencing, we extracted the sites that were covered by high-quality reads (at least six of nine individuals covered by >2X reads). To prepare for ∂a∂i program, we called 1,420,399 SNPs using a published method [69]. The little egret reference genome sequence was used to infer ancestral alleles.…”
Section: Resequencing Data Analysismentioning
confidence: 99%
“…Li et al, 2013;Qu et al, 2013;Li et al, 2014). EGLN1 (1egl 9 homolog 1), PPARA (peroxisome proliferator-activated receptor-a genes) and EPAS1, also known as HIF2α (endothelial PAS domain 1) were significantly associated with hypoxia adaptation (Beall et al, 2010;Bigham et al, 2010;Simonson et al, 2010;Storz, 2010;Yi et al, 2010). However, few studies have been performed on poikilothermic species.…”
Section: Introductionmentioning
confidence: 99%