Discriminating somatic and germline mutations in tumor DNA samples without matching normals

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Figure 1.
Figure 1.

Comparison of matched normal (MN) and virtual normal (VN) methods for structural variations (SVs). Correction of high-confidence SVs from Complete Genomics (left) and Illumina (right), using the database filter (DB), MN, and VN. Light gray area indicates the golden set (combination of the three).

This Article

  1. Published in Advance July 24, 2015, doi: 10.1101/gr.183053.114 Genome Res. 25: 1382-1390

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