Use of molecular variation in the NCBI dbSNP database

42Citations
Citations of this article
50Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

While high quality information regarding variation in genes is currently available in locus-specific or specialized mutation databases, the need remains for a general catalog of genome variation to address the large-scale sampling designs required by association studies, gene mapping, and evolutionary biology. In response to this need, the National Center for Biotechnology Information (NCBI) has established the dbSNP database http://ncbi.nlm.nih.gov/SNP/ to serve as a generalized, central variation database. Submissions to dbSNP will be integrated with other sources of information at NCBI such as GenBank, PubMed, LocusLink, and the Human Genome Project data, and the complete contents of dbSNP are available to the public via anonymous FTP.

Author supplied keywords

Cite

CITATION STYLE

APA

Sherry, S. T., Ward, M., & Sirotkin, K. (2000). Use of molecular variation in the NCBI dbSNP database. Human Mutation, 15(1), 68–75. https://doi.org/10.1002/(SICI)1098-1004(200001)15:1<68::AID-HUMU14>3.0.CO;2-6

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free