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Variations on a Theme: Cataloging Human DNA Sequence Variation
Abstract
New methods for the discovery and scoring of single-nucleotide polymorphisms (SNPs) offer the potential for considerably improved methods for genetic analysis of complex biological phenomena, particularly common diseases. In this Policy Forum, the authors call for a publicly supported effort to discover a large number of SNPs and to place the information in public databases. Participation in this public effort by the private sector would be particularly desirable.
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Metadata
- Authors
- Collins, F. S., Guyer, M. S., & Chakravarti, A.
- Venue
- Science
- Published
- 1997-11-28
- Volume
- 278
- Issue
- 5343
- Pages
- 1580-1581
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2074754379
- Cited by
- 1,050
- References
- 0
- FWCI
- 37.24
- Type
- journal article
- Language
- en
- Open access
- closed
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