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Siberian genetic diversity reveals complex origins of the Samoyedic-speaking populations. / Karafet, Tatiana M.; Osipova, Ludmila P.; Savina, Olga V. et al.

In: American Journal of Human Biology, Vol. 30, No. 6, 23194, 01.11.2018.

Research output: Contribution to journalArticlepeer-review

Harvard

Karafet, TM, Osipova, LP, Savina, OV, Hallmark, B & Hammer, MF 2018, 'Siberian genetic diversity reveals complex origins of the Samoyedic-speaking populations', American Journal of Human Biology, vol. 30, no. 6, 23194. https://doi.org/10.1002/ajhb.23194

APA

Karafet, T. M., Osipova, L. P., Savina, O. V., Hallmark, B., & Hammer, M. F. (2018). Siberian genetic diversity reveals complex origins of the Samoyedic-speaking populations. American Journal of Human Biology, 30(6), [23194]. https://doi.org/10.1002/ajhb.23194

Vancouver

Karafet TM, Osipova LP, Savina OV, Hallmark B, Hammer MF. Siberian genetic diversity reveals complex origins of the Samoyedic-speaking populations. American Journal of Human Biology. 2018 Nov 1;30(6):23194. doi: 10.1002/ajhb.23194

Author

Karafet, Tatiana M. ; Osipova, Ludmila P. ; Savina, Olga V. et al. / Siberian genetic diversity reveals complex origins of the Samoyedic-speaking populations. In: American Journal of Human Biology. 2018 ; Vol. 30, No. 6.

BibTeX

@article{bca5be62c6654de1859d88c52b578a11,
title = "Siberian genetic diversity reveals complex origins of the Samoyedic-speaking populations",
abstract = "Objectives: We examined autosomal genome-wide SNPs and Y-chromosome data from 15 Siberian and 12 reference populations to study the affinities of Siberian populations, and to address hypotheses about the origin of the Samoyed peoples. Methods: Samples were genotyped for 567 096 autosomal SNPs and 147 Y-chromosome polymorphic sites. For several analyses, we used 281 093 SNPs from the intersection of our data with publicly available ancient Siberian samples. To examine genetic relatedness among populations, we applied PCA, FST, TreeMix, and ADMIXTURE analyses. To explore the potential effect of demography and evolutionary processes, the distribution of ROH and IBD sharing within population were studied. Results: Analyses of autosomal and Y-chromosome data reveal high differentiation of the Siberian groups. The Siberian populations have a large proportion of their genome in ROH and IBD segments. Several populations (ie, Nganasans, Evenks, Yukagirs, and Koryaks) do not appear to have experienced admixture with other Siberian populations (ie, producing only positive f3), while for the other tested populations the composition of mixing sources always included Nganasans or Evenks. The Nganasans from the Taymyr Peninsula demonstrate the greatest level of shared shorter ROH and IBD with nearly all other Siberian populations. Conclusions: Autosomal SNP and Y-chromosome data demonstrate that Samoyedic populations differ significantly in their genetic composition. Genetic relationship is observed only between Forest and Tundra Nentsi. Selkups are affiliated with the Kets from the Yenisey River, while the Nganasans are separated from their linguistic neighbors, showing closer affinities with the Evenks and Yukagirs.",
keywords = "MITOCHONDRIAL-DNA, AGE, HISTORY, ADMIXTURE, POLYMORPHISMS, NGANASANS, MIGRATION, LANGUAGES, ANCESTRY, PATTERNS, DNA, Ancient/analysis, Humans, Chromosomes, Human, Y/genetics, Genetic Variation, Siberia, Linguistics, Polymorphism, Single Nucleotide, Human Migration",
author = "Karafet, {Tatiana M.} and Osipova, {Ludmila P.} and Savina, {Olga V.} and Brian Hallmark and Hammer, {Michael F.}",
note = "Publisher Copyright: {\textcopyright} 2018 Wiley Periodicals, Inc.",
year = "2018",
month = nov,
day = "1",
doi = "10.1002/ajhb.23194",
language = "English",
volume = "30",
journal = "American Journal of Human Biology",
issn = "1042-0533",
publisher = "Wiley-Liss Inc.",
number = "6",

}

RIS

TY - JOUR

T1 - Siberian genetic diversity reveals complex origins of the Samoyedic-speaking populations

AU - Karafet, Tatiana M.

AU - Osipova, Ludmila P.

AU - Savina, Olga V.

AU - Hallmark, Brian

AU - Hammer, Michael F.

N1 - Publisher Copyright: © 2018 Wiley Periodicals, Inc.

PY - 2018/11/1

Y1 - 2018/11/1

N2 - Objectives: We examined autosomal genome-wide SNPs and Y-chromosome data from 15 Siberian and 12 reference populations to study the affinities of Siberian populations, and to address hypotheses about the origin of the Samoyed peoples. Methods: Samples were genotyped for 567 096 autosomal SNPs and 147 Y-chromosome polymorphic sites. For several analyses, we used 281 093 SNPs from the intersection of our data with publicly available ancient Siberian samples. To examine genetic relatedness among populations, we applied PCA, FST, TreeMix, and ADMIXTURE analyses. To explore the potential effect of demography and evolutionary processes, the distribution of ROH and IBD sharing within population were studied. Results: Analyses of autosomal and Y-chromosome data reveal high differentiation of the Siberian groups. The Siberian populations have a large proportion of their genome in ROH and IBD segments. Several populations (ie, Nganasans, Evenks, Yukagirs, and Koryaks) do not appear to have experienced admixture with other Siberian populations (ie, producing only positive f3), while for the other tested populations the composition of mixing sources always included Nganasans or Evenks. The Nganasans from the Taymyr Peninsula demonstrate the greatest level of shared shorter ROH and IBD with nearly all other Siberian populations. Conclusions: Autosomal SNP and Y-chromosome data demonstrate that Samoyedic populations differ significantly in their genetic composition. Genetic relationship is observed only between Forest and Tundra Nentsi. Selkups are affiliated with the Kets from the Yenisey River, while the Nganasans are separated from their linguistic neighbors, showing closer affinities with the Evenks and Yukagirs.

AB - Objectives: We examined autosomal genome-wide SNPs and Y-chromosome data from 15 Siberian and 12 reference populations to study the affinities of Siberian populations, and to address hypotheses about the origin of the Samoyed peoples. Methods: Samples were genotyped for 567 096 autosomal SNPs and 147 Y-chromosome polymorphic sites. For several analyses, we used 281 093 SNPs from the intersection of our data with publicly available ancient Siberian samples. To examine genetic relatedness among populations, we applied PCA, FST, TreeMix, and ADMIXTURE analyses. To explore the potential effect of demography and evolutionary processes, the distribution of ROH and IBD sharing within population were studied. Results: Analyses of autosomal and Y-chromosome data reveal high differentiation of the Siberian groups. The Siberian populations have a large proportion of their genome in ROH and IBD segments. Several populations (ie, Nganasans, Evenks, Yukagirs, and Koryaks) do not appear to have experienced admixture with other Siberian populations (ie, producing only positive f3), while for the other tested populations the composition of mixing sources always included Nganasans or Evenks. The Nganasans from the Taymyr Peninsula demonstrate the greatest level of shared shorter ROH and IBD with nearly all other Siberian populations. Conclusions: Autosomal SNP and Y-chromosome data demonstrate that Samoyedic populations differ significantly in their genetic composition. Genetic relationship is observed only between Forest and Tundra Nentsi. Selkups are affiliated with the Kets from the Yenisey River, while the Nganasans are separated from their linguistic neighbors, showing closer affinities with the Evenks and Yukagirs.

KW - MITOCHONDRIAL-DNA

KW - AGE

KW - HISTORY

KW - ADMIXTURE

KW - POLYMORPHISMS

KW - NGANASANS

KW - MIGRATION

KW - LANGUAGES

KW - ANCESTRY

KW - PATTERNS

KW - DNA, Ancient/analysis

KW - Humans

KW - Chromosomes, Human, Y/genetics

KW - Genetic Variation

KW - Siberia

KW - Linguistics

KW - Polymorphism, Single Nucleotide

KW - Human Migration

UR - http://www.scopus.com/inward/record.url?scp=85056152764&partnerID=8YFLogxK

U2 - 10.1002/ajhb.23194

DO - 10.1002/ajhb.23194

M3 - Article

C2 - 30408262

AN - SCOPUS:85056152764

VL - 30

JO - American Journal of Human Biology

JF - American Journal of Human Biology

SN - 1042-0533

IS - 6

M1 - 23194

ER -

ID: 17488113