Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma
Abstract Background In the clinical setting, workflows for analyzing individual genomics data should be both comprehensive and convenient for clinical interpretation. In an effort for comprehensiveness and practicality, we attempted to create a clinical individual whole exome sequencing (WES) analys...
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| Main Authors: | , , , , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2021-02-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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