个人基因组学
基因组
基因组学
数据共享
数据科学
基因组计划
医疗保健
人类基因组
生物
计算机科学
遗传学
政治学
医学
替代医学
病理
基因
法学
作者
Jeantine E. Lunshof,Jason Bobe,John Aach,Misha Angrist,Joseph V. Thakuria,Daniel B. Vorhaus,Margret R. Hoehe,George M. Church
标识
DOI:10.31887/dcns.2010.12.1/jlunshof
摘要
The cost of a diploid human genome sequence has dropped from about $70M to $2000 since 2007--even as the standards for redundancy have increased from 7x to 40x in order to improve call rates. Coupled with the low return on investment for common single-nucleotide polylmorphisms, this has caused a significant rise in interest in correlating genome sequences with comprehensive environmental and trait data (GET). The cost of electronic health records, imaging, and microbial, immunological, and behavioral data are also dropping quickly. Sharing such integrated GET datasets and their interpretations with a diversity of researchers and research subjects highlights the need for informed-consent models capable of addressing novel privacy and other issues, as well as for flexible data-sharing resources that make materials and data available with minimum restrictions on use. This article examines the Personal Genome Project's effort to develop a GET database as a public genomics resource broadly accessible to both researchers and research participants, while pursuing the highest standards in research ethics.
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