Genomic Research and Human Subject Privacy
Top Cited Papers
- 9 July 2004
- journal article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 305 (5681) , 183
- https://doi.org/10.1126/science.1095019
Abstract
Public genetic sequence databases are a critical part of our academic biomedical research infrastructure. However, human genetic data should only be made public if we can adequately protect the privacy of research subjects. Individual genomic sequence data (such as SNPs) are quite "identifiable" using common definitions, while our efforts to understand disease susceptibility or therapeutic opportunity require access to large genomic data sets. The authors of this Policy Forum argue that surprisingly small amounts of genomic sequence data are identifiable. Therefore, the special privacy challenges posed by genomic data need to be addressed with new policies or creative technical approaches.Keywords
This publication has 10 references indexed in Scilit:
- Monitoring ethical, legal, and social issues in developing population genetic databasesGenetics in Medicine, 2003
- UK Biobank: a project in search of a protocol?The Lancet, 2003
- Genetic PrivacyAnnual Review of Medicine, 2003
- Trends in DNA forensic analysisElectrophoresis, 2002
- Privacy and Confidentiality of Genetic Information: What Rules for the New Science?Annual Review of Genomics and Human Genetics, 2001
- Integrating genotype and phenotype information: an overview of the PharmGKB projectThe Pharmacogenomics Journal, 2001
- Elements of Statistical Disclosure ControlPublished by Springer Nature ,2001
- Estonia Prepares for National DNA DatabaseScience, 2000
- The Icelandic database---do modern times need modern sagas?BMJ, 1999
- Low nucleotide diversity in man.Genetics, 1991