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

SNP Function Portal: a web database for exploring the function implication of SNP alleles.

Bioinformatics (Oxford, England) - 15 Jul 2006

Wang Pinglang, Dai Manhong, Xuan Weijian, McEachin Richard C, Jackson Anne U, Scott Laura J, Athey Brian, Watson Stanley J, Meng Fan

Abstract excerpt

MOTIVATION: Finding the potential functional significance of SNPs is a major bottleneck in understanding genome-wide SNP scanning results, as the related functional data are distributed across many different databases. The SNP Function Portal is designed to be a clearing house for all public domain SNP functional annotation data, as well as in-house functional annotations derived from different data sources. It...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Database Management Systems

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

Share to Databases, Genetic

Share to DNA Mutational Analysis

Share to Genome, Human

Share to Information Storage and Retrieval

Share to Internet

Share to User-Computer Interface

Source

Identifiers

PMID: 16873516
DOI: 10.1093/bioinformatics/btl241

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

SNP Function Portal: a web database for exploring the function implication of SNP alleles.PMID 16873516Read ↗

SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies.Semantic proximity Read ↗

F-SNP: computationally predicted functional SNPs for disease association studies.Semantic proximity Read ↗

SNPLogic: an interactive single nucleotide polymorphism selection, annotation, and prioritization system.Semantic proximity Read ↗

A practical guide for the functional annotation of genetic variations using SNPnexus.Semantic proximity Read ↗

pfSNP: An integrated potentially functional SNP resource that facilitates hypotheses generation through knowledge syntheses.Semantic proximity Read ↗

SNP@Promoter: a database of human SNPs (single nucleotide polymorphisms) within the putative promoter regions.Semantic proximity Read ↗

GWASdb: a database for human genetic variants identified by genome-wide association studies.Semantic proximity Read ↗

SNPedia: a wiki supporting personal genome annotation, interpretation and analysis.Semantic proximity Read ↗

A web-based tool to retrieve human genome polymorphisms from public databases.Semantic proximity Read ↗

SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms.Semantic proximity Read ↗

Target SNP selection in complex disease association studies.Semantic proximity Read ↗

SNP-SIG Meeting 2011: identification and annotation of SNPs in the context of structure, function, and disease.Semantic proximity Read ↗

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