Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1756-994X
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
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
- Urheber
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Homburger, Julian R.
Neben, Cynthia L.
Mishne, Gilad
Zhou, Alicia Y.
Kathiresan, Sekar
Khera, Amit V.
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
-
10.1186/s13073-019-0682-2
- URN
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urn:nbn:de:101:1-2020032121210278709426
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:51 MESZ
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Beteiligte
- Homburger, Julian R.
- Neben, Cynthia L.
- Mishne, Gilad
- Zhou, Alicia Y.
- Kathiresan, Sekar
- Khera, Amit V.
- SpringerLink (Online service)
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