| Literature DB >> 27457361 |
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Abstract
The FDA has published two draft guidance documents aimed at streamlining its oversight of tests based on next-generation sequencing (NGS). One contains preliminary recommendations addressing the analytic validity of NGS-based tests for hereditary diseases; the other explains how test developers can obtain official recognition of their genetic variant databases, potentially speeding marketing clearance or approval. ©2016 American Association for Cancer Research.Entities:
Mesh:
Year: 2016 PMID: 27457361 DOI: 10.1158/2159-8290.CD-NB2016-096
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397