Affiliations 

  • 1 Wellcome Sanger Institute, Hinxton CB10 1SA, UK. ab34@sanger.ac.uk cts@sanger.ac.uk
  • 2 Wellcome Sanger Institute, Hinxton CB10 1SA, UK
  • 3 Department of Genetics, University of Cambridge, Cambridge CB2 3EH, UK
  • 4 Centre d'Etude du Polymorphisme Humain, Fondation Jean Dausset, 75010 Paris, France
  • 5 Department of Genetics, Harvard Medical School, Boston, MA 02115, USA
  • 6 The Francis Crick Institute, London NW1 1AT, UK
Science, 2020 Mar 20;367(6484).
PMID: 32193295 DOI: 10.1126/science.aay5012

Abstract

Genome sequences from diverse human groups are needed to understand the structure of genetic variation in our species and the history of, and relationships between, different populations. We present 929 high-coverage genome sequences from 54 diverse human populations, 26 of which are physically phased using linked-read sequencing. Analyses of these genomes reveal an excess of previously undocumented common genetic variation private to southern Africa, central Africa, Oceania, and the Americas, but an absence of such variants fixed between major geographical regions. We also find deep and gradual population separations within Africa, contrasting population size histories between hunter-gatherer and agriculturalist groups in the past 10,000 years, and a contrast between single Neanderthal but multiple Denisovan source populations contributing to present-day human populations.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.