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

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

Bioinformatics (Oxford, England) - 1 Mar 2009

Chelala Claude, Khan Arshad, Lemoine Nicholas R

Abstract excerpt

MOTIVATION: Design a new computational tool allowing scientists to functionally annotate newly discovered and public domain single nucleotide polymorphisms in order to help in prioritizing targets in further disease studies and large-scale genotyping projects. SUMMARY: SNPnexus database provides functional annotation for both novel and public SNPs. Possible effects on the transcriptome and proteome levels are...

Read the complete abstract on PubMed

Topics

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

Share to Databases, Nucleic Acid
Share to Genotype
Share to Internet

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Single Nucleotide

Share to Regulatory Elements, Transcriptional

Source

Open in PubMed Open full text

Identifiers

PMID: 19098027
DOI: 10.1093/bioinformatics/btn653
PMCID: PMC2647830

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms.PMID 19098027Read ↗

SNPnexus: a web server for functional annotation of novel and publicly known genetic variants (2012 update).Semantic proximity Read ↗

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

SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine.Semantic proximity Read ↗

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

SNPnexus: a web server for functional annotation of human genome sequence variation (2020 update).Semantic proximity Read ↗

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

Bioinformatics approaches and resources for single nucleotide polymorphism functional analysis.Semantic proximity Read ↗

Bioinformatics tools for single nucleotide polymorphism discovery and analysis.Semantic proximity Read ↗

FESD: a Functional Element SNPs Database in human.Semantic proximity Read ↗

Current trend of annotating single nucleotide variation in humans--A case study on SNVrap.Semantic proximity Read ↗

LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources.Semantic proximity Read ↗

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

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