Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1530-0366

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing ; volume:22 ; number:11 ; day:6 ; month:7 ; year:2020 ; pages:1892-1897 ; date:11.2020
Genetics in medicine ; 22, Heft 11 (6.7.2020), 1892-1897, 11.2020

Creator: Thibodeau, My Linh
O’Neill, Kieran
Dixon, Katherine
Reisle, Caralyn
Mungall, Karen L.
Krzywinski, Martin
Shen, Yaoqing
Lim, Howard J.
Cheng, Dean
Tse, Kane
Wong, Tina
Chuah, Eric
Fok, Alexandra
Sun, Sophie
Renouf, Daniel
Schaeffer, David F.
Cremin, Carol
Chia, Stephen
Young, Sean
Pandoh, Pawan
Pleasance, Stephen
Pleasance, Erin
Mungall, Andrew J.
Moore, Richard
Yip, Stephen
Karsan, Aly
Laskin, Janessa
Marra, Marco A.
Schrader, Kasmintan A.
Jones, Steven J. M.

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41436-020-0880-8

URN: urn:nbn:de:101:1-2020121208513165473360

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

Last update: 15.08.2025, 7:34 AM CEST

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Associated

Thibodeau, My Linh
O’Neill, Kieran
Dixon, Katherine
Reisle, Caralyn
Mungall, Karen L.
Krzywinski, Martin
Shen, Yaoqing
Lim, Howard J.
Cheng, Dean
Tse, Kane
Wong, Tina
Chuah, Eric
Fok, Alexandra
Sun, Sophie
Renouf, Daniel
Schaeffer, David F.
Cremin, Carol
Chia, Stephen
Young, Sean
Pandoh, Pawan
Pleasance, Stephen
Pleasance, Erin
Mungall, Andrew J.
Moore, Richard
Yip, Stephen
Karsan, Aly
Laskin, Janessa
Marra, Marco A.
Schrader, Kasmintan A.
Jones, Steven J. M.
SpringerLink (Online service)

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Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing

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Other Objects (12)

Local read haplotagging enables accurate long-read small variant calling

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Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes

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Advances in long-read single-cell transcriptomics

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Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes

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