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

WAVe: web analysis of the variome.

Human mutation - 1 Jul 2011

Lopes Pedro, Dalgleish Raymond, Oliveira José Luís

Abstract excerpt

DNA sequence variation is the underlying basis of common human traits and rarer single-gene disorders. Understanding the variome, the variants in an individual's genome, is essential to enable the ultimate goals of personalized medicine. This critical research field has grown dramatically in rece...

Read the complete abstract on PubMed

Topics

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

Share to Databases, Genetic
Share to Genetic Association Studies
Share to Genome, Human

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Individuality

Share to Internet

Share to Precision Medicine

Share to Software

Share to Systems Integration

Source

Identifiers

PMID: 21394829
DOI: 10.1002/humu.21499

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21394829-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

WAVe: web analysis of the variome.PMID 21394829Read ↗

Variobox: automatic detection and annotation of human genetic variants.Semantic proximity Read ↗

The Human Variome Project.Semantic proximity Read ↗

Varietas: a functional variation database portal.Semantic proximity Read ↗

GENETICS. The Human Variome Project.Semantic proximity Read ↗

Human Variome Project Quality Assessment Criteria for Variation Databases.Semantic proximity Read ↗

MobiDetails: online DNA variants interpretation.Semantic proximity Read ↗

Bioinformatics for personal genome interpretation.Semantic proximity Read ↗

VarSome: The Human Genomic Variant Search EngineSemantic proximity Read ↗

Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project.Semantic proximity Read ↗

Practical guidelines addressing ethical issues pertaining to the curation of human locus-specific variation databases (LSDBs).Semantic proximity Read ↗

Human genotype-phenotype databases: aims, challenges and opportunities.Semantic proximity Read ↗

Varapp: A reactive web-application for variants filteringSemantic proximity Read ↗

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