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Computational approaches to identify functional genetic variants in cancer genomes

by Stuart, Josh M , Sander, Chris , Shannon, Nick B , Reva, Boris , Ritchie, Graham R S , Kassahn, Karin S , Valencia, Alfonso , Linding, Rune , Stein, Lincoln D , Muthuswamy, Lakshmi , Ding, Li , Boutros, Paul C , Reimand, Jüri , Carter, Hannah , Creixell, Pau , Vazquez, Miguel , Bader, Gary D , Fink, J Lynn , Mustonen, Ville , Gonzalez-Perez, Abel , Karchin, Rachel , Dronov, Serge , Ouellette, B F Francis , Lopez-Bigas, Nuria , Flicek, Paul , Butler, Adam , Pearson, John V , Shibata, Tatsuhiro

in 631/114 / 631/1647/514/2184 / 631/208/726/649 / 631/67/69 / Bioinformatics / Biological Microscopy / Biological Techniques / Biomedical Engineering/Biotechnology / Cancer / Computational biology / Computational Biology - methods / Genetic aspects / Genetic variance / Genetic Variation / Genome, Human / Genomics / Genotype & phenotype / Humans / Life Sciences / Mutation / Neoplasms - genetics / perspective / Physiological aspects / Proteomics / Tumors

2013

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2013

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2013

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Journal Article

Computational approaches to identify functional genetic variants in cancer genomes

Stuart, Josh M,

Sander, Chris,

Shannon, Nick B,

Reva, Boris,

Ritchie, Graham R S,

Kassahn, Karin S,

Valencia, Alfonso,

Linding, Rune,

Stein, Lincoln D,

Muthuswamy, Lakshmi,

Ding, Li,

Boutros, Paul C,

Reimand, Jüri,

Carter, Hannah,

Creixell, Pau,

Vazquez, Miguel,

Bader, Gary D,

Fink, J Lynn,

Mustonen, Ville,

Gonzalez-Perez, Abel,

Karchin, Rachel,

Dronov, Serge,

Ouellette, B F Francis,

Lopez-Bigas, Nuria,

Flicek, Paul,

Butler, Adam,

Pearson, John V,

Shibata, Tatsuhiro

2013

Overview

International Cancer Genome Consortium members review and recommend computational approaches for identifying mutations that drive cancer progression from among the many sequence variants present in tumor genomes. The International Cancer Genome Consortium (ICGC) aims to catalog genomic abnormalities in tumors from 50 different cancer types. Genome sequencing reveals hundreds to thousands of somatic mutations in each tumor but only a minority of these drive tumor progression. We present the result of discussions within the ICGC on how to address the challenge of identifying mutations that contribute to oncogenesis, tumor maintenance or response to therapy, and recommend computational techniques to annotate somatic variants and predict their impact on cancer phenotype.

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Publisher

Nature Publishing Group US,Nature Publishing Group

Subject

/ Biological Microscopy

/ Biological Techniques