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

snpXplorer: a web application to explore human SNP-associations and annotate SNP-sets.

Nucleic acids research - 2 Jul 2021

Tesi Niccolo, van der Lee Sven, Hulsman Marc, Holstege Henne, Reinders Marcel J T

Abstract excerpt

Genetic association studies are frequently used to study the genetic basis of numerous human phenotypes. However, the rapid interrogation of how well a certain genomic region associates across traits as well as the interpretation of genetic associations is often complex and requires the integration of multiple sources of annotation, which involves advanced bioinformatic skills. We developed snpXplorer, an...

Read the complete abstract on PubMed

Topics

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

Share to Alzheimer Disease
Share to Gene Expression
Share to Genetic Association Studies

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

Share to Genomics

Share to Linkage Disequilibrium

Share to Molecular Sequence Annotation

Share to Quantitative Trait Loci

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 34048563
DOI: 10.1093/nar/gkab410
PMCID: PMC8262737

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

snpXplorer: a web application to explore human SNP-associations and annotate SNP-sets.PMID 34048563Read ↗

<i>snpXplorer</i> : a web application to explore SNP-associations and annotate SNP-setsSemantic proximity Read ↗

snpXplorer: an interactive platform for haplotype-aware exploration and integrated annotation of GWAS dataSemantic proximity Read ↗

GRASP v2.0: an update on the Genome-Wide Repository of Associations between SNPs and phenotypes.Semantic proximity Read ↗

PheLiGe: an interactive database of billions of human genotype-phenotype associations.Semantic proximity Read ↗

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

SNPsnap: a Web-based tool for identification and annotation of matched SNPs.Semantic proximity Read ↗

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

The NHGRI-EBI GWAS Catalog, a curated resource of SNP-trait associationsSemantic proximity Read ↗

SNPper: retrieval and analysis of human SNPs.Semantic proximity Read ↗

Selecting single-nucleotide polymorphisms for association studies with SNPbrowser software.Semantic proximity Read ↗

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations.Semantic proximity Read ↗

Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics.Semantic proximity Read ↗

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