2015
DOI: 10.1101/034983
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Refining the Y chromosome phylogeny with southern African sequences

Abstract: haplogroup B2a is traditionally associated with the spread of Bantu speakers, we find that it probably also existed in Khoisan groups before the arrival of Bantu speakers. Finally, there is pronounced variation in branch length between major haplogroups; in particular, haplogroups associated with Bantu speakers have significantly longer branches. Technical artifacts cannot explain this branch length variation, which instead likely reflects aspects of the demographic history of Bantu speakers, such as recent po… Show more

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Cited by 14 publications
(44 citation statements)
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References 49 publications
(85 reference statements)
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“…We identified single nucleotide variants (SNVs) using GATK UnifiedGenotyper v3.3-0 across all samples simultaneously setting the parameter ploidy to 1 and using DBSNP build 138 as a prior position list. The identified SNVs were further filtered as previously described 54 . We imputed all samples with missing genotype information at any of these variant sites using BEAGLE 55 .…”
Section: Y Chromosomementioning
confidence: 99%
“…We identified single nucleotide variants (SNVs) using GATK UnifiedGenotyper v3.3-0 across all samples simultaneously setting the parameter ploidy to 1 and using DBSNP build 138 as a prior position list. The identified SNVs were further filtered as previously described 54 . We imputed all samples with missing genotype information at any of these variant sites using BEAGLE 55 .…”
Section: Y Chromosomementioning
confidence: 99%
“…In this study, we compare new data on MSY sequence variation with our previous findings on whole mtDNA genomes [9] to investigate whether the histories of these groups fit the expectations of earlier anthropological and linguistic hypotheses, and to study the causes and consequences of sex-biased processes for their genetic variation. [7,27,30]. Main haplogroup clades and their labels are shown with different colors.…”
Section: Introductionmentioning
confidence: 99%
“…We identified single nucleotide variants (SNVs) using GATK UnifiedGenotyper v3.3-0 across all samples simultaneously, setting the parameter ploidy to 1 and using DBSNP build 138 as a prior position list. The identified SNVs were further filtered as previously described by Barbieri et al (2016) (Barbieri et al 2016) and we obtained a set of 2969 SNVs. We imputed all samples with missing genotype information at any of these variant sites using BEAGLE (Browning and Browning 2013) and assigned Y chromosome haplogroups using yhaplo (Poznik et al 2016).…”
Section: Dna Sequencing and Sequence Analysismentioning
confidence: 99%