ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1756-994X

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data ; volume:13 ; number:1 ; day:25 ; month:2 ; year:2021 ; pages:1-19 ; date:12.2021
Genome medicine ; 13, Heft 1 (25.2.2021), 1-19, 12.2021

Creator: Minoche, Andre E.
Lundie, Ben
Peters, Greg B.
Ohnesorg, Thomas
Pinese, Mark
Thomas, David M.
Zankl, Andreas
Roscioli, Tony
Schonrock, Nicole
Kummerfeld, Sarah
Burnett, Leslie
Dinger, Marcel E.
Cowley, Mark J.

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13073-021-00841-x

URN: urn:nbn:de:101:1-2021042221335404728027

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 11:02 AM CEST

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Associated

Minoche, Andre E.
Lundie, Ben
Peters, Greg B.
Ohnesorg, Thomas
Pinese, Mark
Thomas, David M.
Zankl, Andreas
Roscioli, Tony
Schonrock, Nicole
Kummerfeld, Sarah
Burnett, Leslie
Dinger, Marcel E.
Cowley, Mark J.
SpringerLink (Online service)

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ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data

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Other Objects (12)

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