[Dal]

Haplotype sharing provides insights into fine-scale population history and disease in Finland
https://www.biorxiv.org/content/early/2017/10/13/200113

[Kenstut]

У нас серьёзные генетические исследования популяции начались от исследования генетических заболеваний. Нашли даже генетическое заболевание, гены каторового может быть маркерами балтского населения.

[Ведьма Ксения]

Here, we present the whole-genome sequencing data for 386 Mongolian individuals which mainly composed of the Buryats and the Khalkha Mongols by average sequencing depth of 17X. We discovered 3.8 million novel single nucleotide polymorphisms (SNPs) which were not previously reported. Moreover, 965,663 SNPs which were rare (minor allele frequency < 0.5%) in the 1000 genome project phase 3 were low frequency or common in our dataset. Series of analysis demonstrated distinctive population structure of the Mongolians from the East Asians. We constructed robust imputation panel for Northern Asian populations which produces great imputation accuracy for rare (mean r2 of 0.82) and low frequency (mean r2 of 0.87) SNPs. We identified significant gene flow from the Buryats to the Finnish which was predicted to be occurred in 1,228 (±87) year. Moreover, 13.38% of Buryat admixture was predicted in the Finnish genome. In summary, this study illustrated advantage of whole-genome sequencing to build reference panels and to study population history.
https://ep70.eventpilotadmin.com/web/page.php?page=IntHtml&project=ASHG17&id=170121296
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Я Бог, со мной Русские
Прото-германцы в Европе не жили. Если есть indogermanische sprachen, значит есть и indoslawishe sprachen

[Kenstut]

Чё это? Буряты спасаясь от Чингисхана до финов добежали?