Election 2016: Voting on Variants.

Cancer Discov

Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, California.

Published: July 2016

Genome sequencing studies increasingly identify variants of unknown significance in provocative genes. Kim and colleagues present a system with which to functionally annotate such variants in a high-throughput, biologically relevant series of assays. Cancer Discov; 6(7); 694-6. ©2016 AACRSee related article by Kim et al., p. 714.

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http://dx.doi.org/10.1158/2159-8290.CD-16-0559DOI Listing

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