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

A DNA polymorphism discovery resource for research on human genetic variation.

Genome research - 1 Dec 1998

Collins F S, Brooks L D, Chakravarti A

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to DNA
Share to Genetic Diseases, Inborn
Share to Genetic Variation
Share to Polymorphism, Genetic

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

Source

Identifiers

PMID: 9872978
DOI: 10.1101/gr.8.12.1229

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

A DNA polymorphism discovery resource for research on human genetic variation.PMID 9872978Read ↗

Human variation databases.Semantic proximity Read ↗

Genetic variation analysis for biomedical researchers: a primer.Semantic proximity Read ↗

Human genetic bi-allelic sequences (HGBASE), a database of intra-genic polymorphisms.Semantic proximity Read ↗

Pharmacogene Variation Consortium: A Global Resource and Repository for Pharmacogene Variation.Semantic proximity Read ↗

A new human genetic resource: a DNA bank established as part of the Avon Longitudinal Study of Pregnancy and Childhood (ALSPAC)Semantic proximity Read ↗

Human genomics: A deep dive into genetic variation.Semantic proximity Read ↗

The Gnomad Consortium Releases First Studies of Human Genetic Variation.Semantic proximity Read ↗

Finding the Rare Pathogenic Variants in a Human Genome.Semantic proximity Read ↗

The Human Genome Diversity Project as a complement to human population genetics.Semantic proximity Read ↗

Human variation database: an open-source database template for genomic discovery.Semantic proximity Read ↗

DNA variations in human and medical genetics: 25 years of my experience.Semantic proximity Read ↗

[Genome-wide SNP typing].Semantic proximity Read ↗

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