Integrating next-generation sequencing into the diagnostic testing of inherited cancer predisposition-Reference-Cited by-同舟云学术

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Integrating next-generation sequencing into the diagnostic testing of inherited cancer predisposition

Published:2013-01 Issue:1 Volume:83 Page:2-6
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Ku CS¹,Cooper DN²,Iacopetta B³,Roukos DH

Affiliation:

1. Department of Medical Epidemiology and Biostatistics; Karolinska Institutet; Stockholm; Sweden

2. Institute of Medical Genetics, School of Medicine; Cardiff University; Cardiff; UK

3. School of Surgery; University of Western Australia; Crawley; Western Australia; Australia

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference29 articles.

1. Unraveling the genetics of cancer: genome sequencing and beyond;Wong;Annu Rev Genomics Hum Genet,2011

2. Advances in understanding cancer genomes through second-generation sequencing;Meyerson;Nat Rev Genet,2010

3. Exome sequencing: dual role as a discovery and diagnostic tool;Ku;Ann Neurol,2012

4. Exome sequencing can improve diagnosis and alter patient management;Dixon-Salazar;Sci Transl Med,2012

5. Clinical application of exome sequencing in undiagnosed genetic conditions;Need;J Med Genet,2012

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