Management of Incidental Findings in Clinical Genomic Sequencing

Joel B. Krier1, Robert C. Green2

1 Genomes2People Research Program, Division of Genetics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, 2 Broad Institute, Boston, Massachusetts
Publication Name:  Current Protocols in Human Genetics
Unit Number:  Unit 9.23
DOI:  10.1002/0471142905.hg0923s87
Online Posting Date:  October, 2015
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Abstract

Genomic sequencing is becoming accurate, fast, and increasingly inexpensive, and is rapidly being incorporated into clinical practice. Incidental or secondary findings, which can occur in large numbers from genomic sequencing, are a potential barrier to the utility of this new technology due to their relatively high prevalence and the lack of evidence or guidelines available to guide their clinical interpretation. This unit reviews the definition, classification, and management of incidental findings from genomic sequencing. The unit focuses on the clinical aspects of handling incidental findings, with an emphasis on the key role of clinical context in defining incidental findings and determining their clinical relevance and utility. © 2015 by John Wiley & Sons, Inc.

Keywords: incidental findings; secondary findings; genomics; sequencing; whole genome; exome

     
 
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Table of Contents

  • Introduction
  • What are Genomic Incidental Findings?
  • Genetic Variation and the Limitations of Genomic Sequencing
  • A Clinical Approach to Incidental Findings
  • Conclusions and Future Directions
  • Acknowledgments
  • Literature Cited
  • Figures
  • Tables
     
 
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Materials

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Literature Cited

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