VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing

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Figure 5.
Figure 5.

Frequent copy number alteration of ovarian cancer genes. Exome-based copy number estimates were used to compute the proportion of ovarian cancer tumors (n = 142) exhibiting amplification or deletion of key ovarian cancer genes. Asterisks (*) indicate significantly altered genes identified from SNP array data in our previous study.

This Article

  1. Published in Advance February 2, 2012, doi: 10.1101/gr.129684.111 Genome Res. 22: 568-576

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