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 server for functional annotation of human genome sequence variation (2020 update).

Nucleic acids research - 2 Jul 2020

Oscanoa Jorge, Sivapalan Lavanya, Gadaleta Emanuela, Dayem Ullah Abu Z, Lemoine Nicholas R, Chelala Claude

Abstract excerpt

SNPnexus is a web-based annotation tool for the analysis and interpretation of both known and novel sequencing variations. Since its last release, SNPnexus has received continual updates to expand the range and depth of annotations provided. SNPnexus has undergone a complete overhaul of the underlying infrastructure to accommodate faster computational times. The scope for data annotation has been substantially...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Variation
Share to Genome, Human

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Internet

Share to Molecular Sequence Annotation

Share to Neoplasms

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 32496546
DOI: 10.1093/nar/gkaa420
PMCID: PMC7319579

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

SNPnexus: a web server for functional annotation of human genome sequence variation (2020 update).PMID 32496546Read ↗

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

SNPnexus: an enhanced web platform for large-scale and multi-sample variant analysis (2025 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 ↗

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

Genome Nexus: A Comprehensive Resource for the Annotation and Interpretation of Genomic Variants in Cancer.Semantic proximity Read ↗

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

dbNSFP v4: a comprehensive database of transcript-specific functional predictions and annotations for human nonsynonymous and splice-site SNVs.Semantic proximity Read ↗

SNiPA: an interactive, genetic variant-centered annotation browser.Semantic proximity Read ↗

FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.Semantic proximity Read ↗

Functional annotation of noncoding sequence variants.Semantic proximity Read ↗

FAVOR: Functional Annotation of Variants Online Resource and Annotator for Variation across the Human GenomeSemantic proximity Read ↗

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