4.7 Article

MultiWaverX: modeling latent sex-biased admixture history

Journal

BRIEFINGS IN BIOINFORMATICS
Volume 23, Issue 5, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbac179

Keywords

sex-biased gene flow; genetic admixture; chromosome X; ancestry; cancellation model

Funding

  1. National Natural Science Foundation of China (NSFC) [32030020, 32041008, 31961130380, 31900418, 11801027]
  2. Chinese Academy of Sciences(CAS) [XDPB17, XDB38000000]
  3. UK Royal Society-Newton Advanced Fellowship [NAF\R1\191094]
  4. Shanghai Municipal Science and Technology Major Project [2017SHZDZX01]
  5. Fundamental Research Funds for the Central Universities [2020RC001]

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This study presents a novel algorithm, MultiWaverX, for modeling complex admixture history with sex-biased gene flow. Application of MultiWaverX to empirical data revealed sex-biased admixture histories in various populations.
Sex-biased gene flow has been common in the demographic history of modern humans. However, the lack of sophisticated methods for delineating the detailed sex-biased admixture process prevents insights into complex admixture history and thus our understanding of the evolutionary mechanisms of genetic diversity. Here, we present a novel algorithm, MultiWaverX, for modeling complex admixture history with sex-biased gene flow. Systematic simulations showed that MultiWaverX is a powerful tool for modeling complex admixture history and inferring sex-biased gene flow. Application of MultiWaverX to empirical data of 17 typical admixed populations in America, Central Asia, and the Middle East revealed sex-biased admixture histories that were largely consistent with the historical records. Notably, fine-scale admixture process reconstruction enabled us to recognize latent sex-biased gene flow in certain populations that would likely be overlooked by much of the routine analysis with commonly used methods. An outstanding example in the real world is the Kazakh population that experienced complex admixture with sex-biased gene flow but in which the overall signature has been canceled due to biased gene flow from an opposite direction.

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