Whole-genome sequencing of triple-negative breast cancers in a population-based clinical study-Reference-Cited by-同舟云学术

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Whole-genome sequencing of triple-negative breast cancers in a population-based clinical study

Published:2019-09-30 Issue:10 Volume:25 Page:1526-1533
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Staaf Johan^ORCID,Glodzik Dominik^ORCID,Bosch Ana,Vallon-Christersson Johan^ORCID,Reuterswärd Christel,Häkkinen Jari^ORCID,Degasperi Andrea^ORCID,Amarante Tauanne Dias^ORCID,Saal Lao H.^ORCID,Hegardt Cecilia,Stobart Hilary,Ehinger Anna^ORCID,Larsson Christer,Rydén Lisa,Loman Niklas,Malmberg Martin,Kvist Anders,Ehrencrona Hans,Davies Helen R.,Borg Åke,Nik-Zainal Serena

Funder

Wellcome Trust

Cancer Research UK

Cancerfonden

Sveriges Regering

Fru Berta Kamprads Stiftelse

Crafoordska Stiftelsen

Stiftelsen Konung Gustaf V:s Jubileumsfond

Vetenskapsrådet

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/s41591-019-0582-4.pdf

Reference35 articles.

1. Bentley, D. R. et al. Accurate whole human genome sequencing using reversible terminator chemistry. Nature 456, 53–59 (2008).

2. Nik-Zainal, S. et al. Mutational processes molding the genomes of 21 breast cancers. Cell 149, 979–993 (2012).

3. Nik-Zainal, S. et al. The life history of 21 breast cancers. Cell 149, 994–1007 (2012).

4. Ryden, L. et al. Minimizing inequality in access to precision medicine in breast cancer by real-time population-based molecular analysis in the SCAN-B initiative. Br. J. Surg. 105, e158–e168 (2018).

5. Saal, L. H. et al. The Sweden Cancerome Analysis Network-Breast (SCAN-B) initiative: a large-scale multicenter infrastructure towards implementation of breast cancer genomic analyses in the clinical routine. Genome Med. 7, 20 (2015).

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