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

DigiPINS: a database for vertebrate exonic single nucleotide polymorphisms and its application to cancer association studies.

Biochimie - 1 Apr 2008

Navratil Vincent, Penel Simon, Delmotte Stéphane, Mouchiroud Dominique, Gautier Christian, Aouacheria Abdel

Abstract excerpt

Single nucleotide polymorphisms (SNPs), which are the most abundant form of genetic variations in numerous organisms, have emerged as important tools for the study of complex genetic traits and deciphering of genome evolution. High-throughput genome sequencing projects worldwide provide an unprecedented opportunity for whole-genome SNP analysis in a variety of species. To facilitate SNP discovery in vertebrates,...

Read the complete abstract on PubMed

Topics

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

Share to Biomarkers
Share to Databases, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Expressed Sequence Tags

Share to Genome

Share to Information Storage and Retrieval

Share to Internet

Share to Software

Share to User-Computer Interface

Source

Identifiers

PMID: 17988782
DOI: 10.1016/j.biochi.2007.09.017

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

DigiPINS: a database for vertebrate exonic single nucleotide polymorphisms and its application to cancer association studies.PMID 17988782Read ↗

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

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

Reliable identification of large numbers of candidate SNPs from public EST data.Semantic proximity Read ↗

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

dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations.Semantic proximity Read ↗

Pharmosome: an integrative and collective database for exploration and analysis of single nucleotide polymorphisms associated with diseaseSemantic proximity Read ↗

ssSNPTarget: genome-wide splice-site Single Nucleotide Polymorphism database.Semantic proximity Read ↗

SNPHunter: a versatile web-based tool for acquiring and managing single nucleotide polymorphisms.Semantic proximity Read ↗

Mining SNPs from DNA sequence data; computational approaches to SNP discovery and analysis.Semantic proximity Read ↗

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

Snap: an integrated SNP annotation platform.Semantic proximity Read ↗

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

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