Whole-Genome and Whole-Exome Sequencing in Hereditary Cancer Impact on Genetic Testing and Counseling

被引:23
|
作者
O'Daniel, Julianne M. [1 ]
Lee, Kristy [2 ]
机构
[1] Illumina Inc, San Diego, CA 92122 USA
[2] Univ N Carolina, Canc & Adult Program, Chapel Hill, NC USA
来源
CANCER JOURNAL | 2012年 / 18卷 / 04期
关键词
Whole genome; whole-genome sequencing; genetic testing; hereditary cancer practice; genetic counseling; whole exome;
D O I
10.1097/PPO.0b013e318262467e
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The incorporation of whole-genome and whole-exome sequencing into clinical practice will undoubtedly change the way genetic counselors and other clinicians approach genetic testing. Enabling the analysis of essentially all human genes in one comprehensive test, this new technology can result in reduced testing cost and time to diagnosis. Another consequence of this broad scope, however, is the increased amount, complexity, and variety of results a clinician may need to discuss with a patient. The purpose of this article is to review the technology and outline some of the benefits and challenges of whole-genome and whole-exome sequencing in hereditary cancer practice.
引用
收藏
页码:287 / 292
页数:6
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