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

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Figure 3.
Figure 3.

Number of structural variants filtered out after each additional VN sample for Complete Genomics (left) and Illumina samples (right). Blue denotes the HCC1187 sample; red, CG HCC2218. Dashed lines indicate the level reached by correction with the associated normal.

This Article

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

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