Review of clinical next-generation sequencing

Research output: Contribution to journalReview articlepeer-review

130 Scopus citations

Abstract

Context.-Next-generation sequencing (NGS) is a technology being used by many laboratories to test for inherited disorders and tumor mutations. This technology is new for many practicing pathologists, who may not be familiar with the uses, methodology, and limitations of NGS. Objective.-To familiarize pathologists with several aspects of NGS, including current and expanding uses; methodology including wet bench aspects, bioinformatics, and interpretation; validation and proficiency; limitations; and issues related to the integration of NGS data into patient care. Data Sources.-The review is based on peer-reviewed literature and personal experience using NGS in a clinical setting at a major academic center. Conclusions.-The clinical applications of NGS will increase as the technology, bioinformatics, and resources evolve to address the limitations and improve quality of results. The challenge for clinical laboratories is to ensure testing is clinically relevant, cost-effective, and can be integrated into clinical care.

Original languageEnglish (US)
Pages (from-to)1544-1557
Number of pages14
JournalArchives of Pathology and Laboratory Medicine
Volume141
Issue number11
DOIs
StatePublished - Nov 2017

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