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Updated: Jul 13, 2025

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Comparative Lesions Analysis Through a Targeted Sequencing Approach
Published on: November 5, 2019
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Clinically significant germline pathogenic variants are missed by tumor genomic sequencing
Leigh Anne Stout1,2, Cynthia Hunter2, Courtney Schroeder2
1Indiana University School of Medicine, Indianapolis, IN, USA.
NPJ Genomic Medicine
|October 13, 2023
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.
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