Whole Genome Sequencing: A Considered Approach to Clinical Implementation. (1st April 2013)

• Record Type: Journal Article
• Authors: Dimmock, David
• Editors: Haines, Jonathan L.; Korf, Bruce R.; Morton, Cynthia C.; Seidman, Christine E.; Seidman, J.G.; Smith, Douglas R.
• Is Part Of: Current protocols in human genetics. Volume 77(2013)
• Page Start: 9.22.1
• Page End: 9.22.7
• Publication Date: 2013-04-01
• Subjects: DNA testing -- clinical implementation -- ethics -- presymptomatic prediction -- data return -- pharmacogenomics -- consent -- genetic counseling; Human genetics -- Laboratory manuals; Genetic Techniques; Human genetics; Laboratory manuals; 599.935028
• DOI: 10.1002/0471142905.hg0922s77
• Languages: English
• ISSNs: 1934-8258

Abstract

Abstract: The recent entry of "whole" exome/"whole" genome sequencing into limited clinical practice has led to a progression of the availability of genome‐scale testing beyond deletion/duplication copy number arrays. This unit provides a considered approach to the implementation of such testing in routine clinical practice. Specifically, we will highlight the challenges in patient selection and consent, and the technical issues surrounding test interpretation and reporting. The unit will then provide practical solutions that allow for genome‐wide sequencing to be implemented in current clinical practice. Curr. Protoc. Hum. Genet . 77:9.22.1‐9.22.7. © 2013 by John Wiley & Sons, Inc.