Strong Maternal Khoisan Contribution to the South African Coloured Population: A Case of Gender-Biased Admixture  Lluis Quintana-Murci, Christine Harmant,

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Strong Maternal Khoisan Contribution to the South African Coloured Population: A Case of Gender-Biased Admixture  Lluis Quintana-Murci, Christine Harmant, Hélène Quach, Oleg Balanovsky, Valery Zaporozhchenko, Connie Bormans, Paul D. van Helden, Eileen G. Hoal, Doron M. Behar  The American Journal of Human Genetics  Volume 86, Issue 4, Pages 611-620 (April 2010) DOI: 10.1016/j.ajhg.2010.02.014 Copyright © 2010 The American Society of Human Genetics Terms and Conditions

Figure 1 Diverse Continental Origins of Maternal and Paternal Contributions to the South African Coloured Bar sizes reflect the combined frequencies of all haplogroups, indicated separately for mtDNA and NRY, associated with the sub-Saharan African, west Eurasian/European, and south/southeast Asian genetic components (Table S1, Tables 1 and 2). The American Journal of Human Genetics 2010 86, 611-620DOI: (10.1016/j.ajhg.2010.02.014) Copyright © 2010 The American Society of Human Genetics Terms and Conditions

Figure 2 MDS Plots Illustrating the Relationships between the South African Coloured Population and the Five Putative Parental Populations (A) MDS plot based on mtDNA Hg frequencies. (B) MDS plot based on NRY Hg frequencies. The five metapopulations used as putative parental populations include Europeans, Indians, Khoisan, Bantu speakers, and southeast Asians. The European dataset included British, French, Dutch, German, and Austrian populations; the Indian dataset included populations from the Bengal Bay coast (Sri Lanka, Bangladesh, and eastern states of India); the Khoisan dataset included all available Khoisan data; the Bantu dataset included Bantu-speaking populations from South Africa and central Africa; and the southeast Asian dataset included populations from the Malay Peninsula, Sumatra, Java, and neighboring smaller isles. Because different individuals and populations have been analyzed for mtDNA and NRY, sample sizes from these metapopulations differ between the two analyses. Sample sizes of European, Indian, Khoisan, Bantu, and southeast Asian populations were, respectively: n = 6092, n = 1246, n = 298, n = 459, and n = 616 for mtDNA and n = 353, n = 766, n = 122, n = 499, and n = 66 for NRY. The lower population sample sizes for the NRY data result from the nonoverlapping nature of the markers used in the different studies. These comparative data were obtained from the MURKA database, compiled from published sources by O. Balanovsky, V. Zaporozhchenko, R. Sychev, A. Pshenichnov, and E. Balanovska. The American Journal of Human Genetics 2010 86, 611-620DOI: (10.1016/j.ajhg.2010.02.014) Copyright © 2010 The American Society of Human Genetics Terms and Conditions

Figure 3 Diverse Continental and within-Continental Admixture Proportions in the South African Coloured Population Mean Khoisan, Bantu-speaking, European, Indian, and southeast Asian admixture proportions among the SAC, on the basis of the mY estimator, are represented as bars for the mtDNA and NRY data. Error bars indicate standard deviations. The five parental metapopulations used for this analysis, as well as their sample sizes, were the same as those used for the MDS analysis (Figure 2). Time of the initial admixture event was set to 400 years, and standard deviations were calculated on the basis of 10,000 bootstraps. The American Journal of Human Genetics 2010 86, 611-620DOI: (10.1016/j.ajhg.2010.02.014) Copyright © 2010 The American Society of Human Genetics Terms and Conditions