Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples
With the generation of large pan-cancer whole-exome and whole-genome sequencing projects, a question remains about how comparable these datasets are. Here, using The Cancer Genome Atlas samples analysed as part of the Pan-Cancer Analysis of Whole Genomes project, the authors explore the concordance...
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Nature Portfolio
2020
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oai:doaj.org-article:d9cb28829f31451aa7d92697e8efd1862021-12-02T18:14:31ZRetrospective evaluation of whole exome and genome mutation calls in 746 cancer samples10.1038/s41467-020-18151-y2041-1723https://doaj.org/article/d9cb28829f31451aa7d92697e8efd1862020-09-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-18151-yhttps://doaj.org/toc/2041-1723With the generation of large pan-cancer whole-exome and whole-genome sequencing projects, a question remains about how comparable these datasets are. Here, using The Cancer Genome Atlas samples analysed as part of the Pan-Cancer Analysis of Whole Genomes project, the authors explore the concordance of mutations called by whole exome sequencing and whole genome sequencing techniques.Matthew H. BaileyWilliam U. MeyersonLewis Jonathan DursiLiang-Bo WangGuanlan DongWen-Wei LiangAmila WeerasingheShantao LiYize LiSean KelsoMC3 Working GroupPCAWG novel somatic mutation calling methods working groupGordon SaksenaKyle EllrottMichael C. WendlDavid A. WheelerGad GetzJared T. SimpsonMark B. GersteinLi DingPCAWG ConsortiumNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-27 (2020) |
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Science Q Matthew H. Bailey William U. Meyerson Lewis Jonathan Dursi Liang-Bo Wang Guanlan Dong Wen-Wei Liang Amila Weerasinghe Shantao Li Yize Li Sean Kelso MC3 Working Group PCAWG novel somatic mutation calling methods working group Gordon Saksena Kyle Ellrott Michael C. Wendl David A. Wheeler Gad Getz Jared T. Simpson Mark B. Gerstein Li Ding PCAWG Consortium Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples |
description |
With the generation of large pan-cancer whole-exome and whole-genome sequencing projects, a question remains about how comparable these datasets are. Here, using The Cancer Genome Atlas samples analysed as part of the Pan-Cancer Analysis of Whole Genomes project, the authors explore the concordance of mutations called by whole exome sequencing and whole genome sequencing techniques. |
format |
article |
author |
Matthew H. Bailey William U. Meyerson Lewis Jonathan Dursi Liang-Bo Wang Guanlan Dong Wen-Wei Liang Amila Weerasinghe Shantao Li Yize Li Sean Kelso MC3 Working Group PCAWG novel somatic mutation calling methods working group Gordon Saksena Kyle Ellrott Michael C. Wendl David A. Wheeler Gad Getz Jared T. Simpson Mark B. Gerstein Li Ding PCAWG Consortium |
author_facet |
Matthew H. Bailey William U. Meyerson Lewis Jonathan Dursi Liang-Bo Wang Guanlan Dong Wen-Wei Liang Amila Weerasinghe Shantao Li Yize Li Sean Kelso MC3 Working Group PCAWG novel somatic mutation calling methods working group Gordon Saksena Kyle Ellrott Michael C. Wendl David A. Wheeler Gad Getz Jared T. Simpson Mark B. Gerstein Li Ding PCAWG Consortium |
author_sort |
Matthew H. Bailey |
title |
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples |
title_short |
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples |
title_full |
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples |
title_fullStr |
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples |
title_full_unstemmed |
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples |
title_sort |
retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples |
publisher |
Nature Portfolio |
publishDate |
2020 |
url |
https://doaj.org/article/d9cb28829f31451aa7d92697e8efd186 |
work_keys_str_mv |
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