Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing
Abstract Background The growing number of Next Generation Sequencing (NGS) tests is transforming the routine clinical diagnosis of hereditary cancers. Identifying whether a cancer is the result of an underlying disease-causing mutation in a cancer predisposition gene is not only diagnostic for a can...
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Main Authors: | , , , , , , , , , , , , , , , , , |
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Format: | Book |
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BMC,
2017-05-01T00:00:00Z.
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A1234.567 |
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