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- W4387637118 abstract "A germline pathogenic variant may be present even if the results of tumor genomic sequencing do not suggest one. There are key differences in the assay design and reporting of variants between germline and somatic laboratories. When appropriate, both tests should be completed to aid in therapy decisions and determining optimal screening and risk-reduction interventions." @default.
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- W4387637118 date "2023-10-13" @default.
- W4387637118 modified "2023-10-18" @default.
- W4387637118 title "Clinically significant germline pathogenic variants are missed by tumor genomic sequencing" @default.
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- W4387637118 doi "https://doi.org/10.1038/s41525-023-00374-9" @default.
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