A method to reduce ancestry related germline false positives in tumor only somatic variant calling
Abstract Background Significant clinical and research applications are driving large scale adoption of individualized tumor sequencing in cancer in order to identify tumors-specific mutations. When a matched germline sample is available, somatic mutations may be identified using comparative callers....
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| Main Authors: | , , , , , , , , , , , , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2017-10-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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