Tools
BioMart >
Export custom datasets from Ensembl with this data-mining tool
BLAST/BLAT >
Search our genomes for your DNA or protein sequence
Variant Effect Predictor >
Analyse your own variants and predict the functional consequences of known and unknown variants
Favourite genomes
Ensembl is a genome browser for vertebrate genomes that supports research in comparative genomics, evolution, sequence variation and transcriptional regulation. Ensembl annotate genes, computes multiple alignments, predicts regulatory function and collects disease data. Ensembl tools include BLAST, BLAT, BioMart and the Variant Effect Predictor (VEP) for all supported species.
Ensembl Release 93 (July 2018)
- Human dbSNP update – twice as many short variants!
- New regulatory build and GENCODE gene set for mouse
- New species: tiger, leopard and hagfish
- New cat assembly and genebuild
- Changes to the VEP REST API endpoints
More release news on our blog
Other news from our blog
- 14 Sep 2018: New variant pathogenicity predictors
- 10 Sep 2018: Ensembl at AfSHG conference, Rwanda
- 06 Sep 2018: Cool stuff the VEP can do: installation
Ensembl creates, integrates and distributes reference datasets and analysis tools that enable genomics. We are based at EMBL-EBI and our software and data are freely available.
Our acknowledgements page includes a list of current and previous funding bodies. How to cite Ensembl in your own publications.
Ensembl release 93 - July 2018 ©
EMBL-EBI
EMBL-EBI
http://www.ensembl.org
.
Get help
.