Copy-number and gene dependency analysis reveals partial copy loss of wild-type SF3B1 as a novel cancer vulnerability
Genomic instability is a hallmark of human cancer, and results in widespread somatic copy number alterations. We used a genome-scale shRNA viability screen in human cancer cell lines to systematically identify genes that are essential in the context of particular copy-number alterations (copy-number...
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Other Authors: | |
Format: | Article |
Language: | en_US |
Published: |
eLife Sciences Publications, Ltd.
2017
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Online Access: | http://hdl.handle.net/1721.1/109875 https://orcid.org/0000-0003-3159-8175 https://orcid.org/0000-0001-5367-2546 |