A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing

Tyler Alioto(Universitat Pompeu Fabra), Ivo Buchhalter(German Cancer Research Center), Sophia Derdak(Universitat Pompeu Fabra), Barbara Hutter(German Cancer Research Center), Matthew Eldridge(University of Cambridge), Eivind Hovig(Oslo University Hospital), Lawrence E. Heisler(Ontario Institute for Cancer Research), Timothy A. Beck(Ontario Institute for Cancer Research), Jared T. Simpson(Ontario Institute for Cancer Research), Laurie Tonon(Centre Léon Bérard), Anne-Sophie Sertier(Centre Léon Bérard), Ann‐Marie Patch(The University of Queensland), Natalie Jäger(German Cancer Research Center), Philip Ginsbach(German Cancer Research Center), Ruben M. Drews(German Cancer Research Center), Nagarajan Paramasivam(German Cancer Research Center), Rolf Kabbe(German Cancer Research Center), Sasithorn Chotewutmontri(German Cancer Research Center), Nicolle Diessl(German Cancer Research Center), Christopher Previti(German Cancer Research Center), Sabine Schmidt(German Cancer Research Center), Benedikt Brors(German Cancer Research Center), Lars Feuerbach(German Cancer Research Center), Michael C. Heinold(German Cancer Research Center), Susanne Gröbner(Heidelberg University), Andrey Korshunov(Heidelberg University), Patrick Tarpey(Wellcome Sanger Institute), Adam P. Butler(Wellcome Sanger Institute), Jonathan Hinton(Wellcome Sanger Institute), David Jones(German Cancer Research Center), Andrew Menzies(Wellcome Sanger Institute), Keiran Raine(Wellcome Sanger Institute), Rebecca Shepherd(Wellcome Sanger Institute), Lucy Stebbings(Wellcome Sanger Institute), Jon W. Teague(Wellcome Sanger Institute), Paolo Ribeca(Universitat Pompeu Fabra), Francesc Castro-Giner(Universitat Pompeu Fabra), Sergi Beltrán(Universitat Pompeu Fabra), Emanuele Raineri(Universitat Pompeu Fabra), Marc Dabad(Universitat Pompeu Fabra), Simon Heath(Universitat Pompeu Fabra), Marta Gut(Universitat Pompeu Fabra), Robert E. Denroche(Ontario Institute for Cancer Research), Nicholas J. Harding(Ontario Institute for Cancer Research), Takafumi N. Yamaguchi(Ontario Institute for Cancer Research), Akihiro Fujimoto(RIKEN Center for Integrative Medical Sciences), Hidewaki Nakagawa(RIKEN Center for Integrative Medical Sciences), Vı́ctor Quesada(Universidad de Oviedo), Rafael Valdés‐Mas(Universidad de Oviedo), Sigve Nakken(Oslo University Hospital), Daniel Vodák(Oslo University Hospital), Lawrence Bower(University of Cambridge), Andy G. Lynch(University of Cambridge), Charlotte Anderson(The University of Melbourne), Nicola Waddell(The University of Queensland), John V. Pearson(The University of Queensland), Sean M. Grimmond(The University of Queensland), Myron Peto(Oregon Health & Science University), Paul T. Spellman(Oregon Health & Science University), Minghui He(BGI Group (China)), Cyriac Kandoth(Washington University in St. Louis), Semin Lee(Harvard University), John H. Zhang(The University of Texas MD Anderson Cancer Center), Louis Létourneau(McGill University), Singer Ma(University of California, Santa Cruz), Sahil Seth(The University of Texas MD Anderson Cancer Center), David Torrents(Barcelona Supercomputing Center), Xi Liu(Baylor College of Medicine), David A. Wheeler(Baylor College of Medicine), Carlos López-Otı́n(Universidad de Oviedo), Elı́as Campo(Consorci Institut D'Investigacions Biomediques August Pi I Sunyer), Peter J. Campbell(Wellcome Sanger Institute), Paul C. Boutros(University of Toronto), Xosé S. Puente(Universidad de Oviedo), Daniela S. Gerhard(National Cancer Institute), Stefan M. Pfister(German Cancer Research Center), John D. McPherson(Ontario Institute for Cancer Research), Thomas J. Hudson(Ontario Institute for Cancer Research), Matthias Schlesner(German Cancer Research Center), Peter Lichter(German Cancer Research Center), Roland Eils(German Cancer Research Center), David Jones(German Cancer Research Center), Marta Gut(Universitat Pompeu Fabra)
Nature Communications
December 9, 2015
Cited by 336Open Access
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Abstract

As whole-genome sequencing for cancer genome analysis becomes a clinical tool, a full understanding of the variables affecting sequencing analysis output is required. Here using tumour-normal sample pairs from two different types of cancer, chronic lymphocytic leukaemia and medulloblastoma, we conduct a benchmarking exercise within the context of the International Cancer Genome Consortium. We compare sequencing methods, analysis pipelines and validation methods. We show that using PCR-free methods and increasing sequencing depth to ∼ 100 × shows benefits, as long as the tumour:control coverage ratio remains balanced. We observe widely varying mutation call rates and low concordance among analysis pipelines, reflecting the artefact-prone nature of the raw data and lack of standards for dealing with the artefacts. However, we show that, using the benchmark mutation set we have created, many issues are in fact easy to remedy and have an immediate positive impact on mutation detection accuracy.


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