Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Use of molecular variation in the NCBI dbSNP database.

Human mutation - 1 Jan 2000

Sherry S T, Ward M, Sirotkin K

Abstract excerpt

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...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Databases, Factual
Share to Evolution, Molecular
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Human Genome Project

Share to Internet

Share to Pharmacogenetics

Share to Polymorphism, Single Nucleotide

Share to United States

Source

Identifiers

PMID: 10612825
DOI: 10.1002/(SICI)1098-1004(200001)15:1<68::AID-HUMU14>3.0.CO;2-6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Use of molecular variation in the NCBI dbSNP database.PMID 10612825Read ↗

dbSNP: the NCBI database of genetic variation.Semantic proximity Read ↗

dbSNP: a database of single nucleotide polymorphisms.Semantic proximity Read ↗

dbSNP-database for single nucleotide polymorphisms and other classes of minor genetic variation.Semantic proximity Read ↗

The evolution of dbSNP: 25 years of impact in genomic research.Semantic proximity Read ↗

Searching NCBI's dbSNP database.Semantic proximity Read ↗

A DNA polymorphism discovery resource for research on human genetic variation.Semantic proximity Read ↗

Single nucleotide differences (SNDs) in the dbSNP database may lead to errors in genotyping and haplotyping studies.Semantic proximity Read ↗

Single nucleotide differences (SNDs) continue to contaminate the dbSNP database with consequences for human genomics and health.Semantic proximity Read ↗

Genome-wide evaluation of the public SNP databases.Semantic proximity Read ↗

Guidelines and recommendations for content, structure, and deployment of mutation databases: II. Journey in progress.Semantic proximity Read ↗

Digital genotyping using molecular affinity and mass spectrometry.Semantic proximity Read ↗

Single-nucleotide polymorphisms in the public domain: how useful are they?Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.