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interrogating the architecture of cancer genomes询问癌症基因组的结构
Genome Biology 2011, 12(Suppl 1)
/supplements/12/S1
M E E T I N G A B S T R AC T S
Beyond the Genome 2011
Washington DC, USA. 19–22 September 2011
Published: 19 September 2011
INVITED SPEAKER PRESENTATIONS I4
Interrogating the architecture of cancer genomes
Peter Campbell
I1 Cancer Genome Project, Wellcome Trust Sanger Institute, Hinxton, UK
Analysis of 2,440 human exomes highlights the evolution and functional Genome Biology 2011, 12(Suppl 1):I11
impact of rare coding variation
Joshua Akey Cancer is driven by mutation. Using massively parallel sequencing technology,
Department of Genome Sciences, University of Washington, Seattle, WA 98195, we can now sequence the entire genome of cancer samples, allowing the
USA generation of comprehensive catalogs of somatic mutations of all classes.
Genome Biology 2011, 12(Suppl 1):I18 Bespoke algorithms have been developed to identify somatically acquired
point mutations, copy number changes and genomic rearrangements, which
Deep exome resequencing is a powerful approach for delineating patterns require extensive validation by coni rmatory testing. The i ndings from our i rst
of
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