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

The Ensembl Variant Effect Predictor.

Genome biology - 6 Jun 2016

McLaren William, Gil Laurent, Hunt Sarah E, Riat Harpreet Singh, Ritchie Graham R S, Thormann Anja, Flicek Paul, Cunningham Fiona

Abstract excerpt

The Ensembl Variant Effect Predictor is a powerful toolset for the analysis, annotation, and prioritization of genomic variants in coding and non-coding regions. It provides access to an extensive collection of genomic annotation, with a variety of interfaces to suit different requirements, and simple options for configuring and extending analysis. It is open source, free to use, and supports full reproducibility...

Read the complete abstract on PubMed

Topics

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

Share to Computational Biology
Share to Databases, Nucleic Acid

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Genomics

Share to Internet

Share to Molecular Sequence Annotation

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 27268795
DOI: 10.1186/s13059-016-0974-4
PMCID: PMC4893825

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

The Ensembl Variant Effect Predictor.PMID 27268795Read ↗

The Ensembl Variant Effect PredictorSemantic proximity Read ↗

Annotating and prioritizing genomic variants using the Ensembl Variant Effect Predictor-A tutorial.Semantic proximity Read ↗

VariantAnnotation: a Bioconductor package for exploration and annotation of genetic variants.Semantic proximity Read ↗

Functional annotation of noncoding sequence variants.Semantic proximity Read ↗

Variant Annotation and Functional Prediction: SnpEff.Semantic proximity Read ↗

Variant effect predictors: a systematic review and practical guide.Semantic proximity Read ↗

Effective variant filtering and expected candidate variant yield in studies of rare human diseaseSemantic proximity Read ↗

VARAdb: a comprehensive variation annotation database for human.Semantic proximity Read ↗

Guidelines for releasing a variant effect predictor.Semantic proximity Read ↗

Variant Impact Predictor database (VIPdb), version 2: trends from three decades of genetic variant impact predictors.Semantic proximity Read ↗

Classification of non-coding variants with high pathogenic impact.Semantic proximity Read ↗

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor.Semantic proximity Read ↗

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