Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores

Location
Deutsche Nationalbibliothek Frankfurt am Main
ISSN
1756-994X
Extent
Online-Ressource
Language
Englisch
Notes
online resource.

Bibliographic citation
Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores ; volume:11 ; number:1 ; day:26 ; month:11 ; year:2019 ; pages:1-12 ; date:12.2019
Genome medicine ; 11, Heft 1 (26.11.2019), 1-12, 12.2019

Creator
Homburger, Julian R.
Neben, Cynthia L.
Mishne, Gilad
Zhou, Alicia Y.
Kathiresan, Sekar
Khera, Amit V.
Contributor
SpringerLink (Online service)

DOI
10.1186/s13073-019-0682-2
URN
urn:nbn:de:101:1-2020032121210278709426
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
09.04.2024, 2:42 PM CEST

Data provider

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Associated

  • Homburger, Julian R.
  • Neben, Cynthia L.
  • Mishne, Gilad
  • Zhou, Alicia Y.
  • Kathiresan, Sekar
  • Khera, Amit V.
  • SpringerLink (Online service)

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