Want to know what’s next for variation data? Join us to explore the latest EVA developments, hear community insights, & help steer the EVA roadmap! 𝟮𝟮 𝗢𝗰𝘁 𝟮𝟬𝟮𝟲 | 𝟭𝟰:𝟬𝟬–𝟭𝟲:𝟬𝟬 𝗕𝗦𝗧 | 𝗙𝗿𝗲𝗲 𝗼𝗻 𝗭𝗼𝗼𝗺 Registration is now open: embl-org.zoom.us/meeting/regi...
Ensembl
@ensembl.org
The Ensembl project seeks to enable genomic science by providing high-quality, integrated annotation.
Ensembl archive sites are currently under very heavy load, causing failures and slow performance. Sorry for the disruptions, we're working on it. Workaround for Ensembl 116 (June 2026): use the Ensembl 115 (Sep 2025) archive instead - sep2025.archive.ensembl.org/index.html
Are you a skilled and highly motivated Bioinformatics Developer looking for a new opportunity? Join the DECIPHER team - gain knowledge of clinical genomics and improved web development skills while creating tools to facilitate genomic medicine. embl.wd103.myworkdayjobs.com/EMBL/job/Hin...
AlphaGenome Variant Impact (AVI) scores, developed by Google DeepMind, predict how likely variants across the whole human genome are to impact gene regulation. AVI scores are available in the Ensembl Variant Effect Predictor to enable easy access into variant analysis workflows.
The new Ensembl VEP web interface just got upgraded for human GRCh38 variants! Add scores from AlphaMissense, REVEL, CADD, and SpliceAI. Link gnomAD frequencies, ClinVar & GWAS Catalog phenotypes to your data. Try it at- ensembl.org/tools/vep Blog- www.ensembl.info/2026/09/04/n...
Want a quick tour of the new Ensembl? Check out our new material on the EMBL-EBI Training site! It's free to access - give it a try and see what genomes are available on Ensembl now. 🧬
Have you tried the new @ensembl.org platform yet? Together with the team, we've put together this quick tour to give you a short introduction to the new Ensembl website for exploring genomes from across the tree of life: www.ebi.ac.uk/training/onl... Learning time: >30 minutes. 🧬🖥️📊🌱
Exciting opportunity to work with Ensembl microbes! We are seeking a bioinformatician to help us develop and maintain high-quality genome resources for microbial research communities. More info: zurl.co/hdKpk #Jobs #bioinformatics
Job: Bioinformatician (Ensembl Microbes team) – Ensembl Blog
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Explore genes & transcripts with the @Ensembl Feature Explorer! Using human BRCA2 as an example, learn how to explore transcripts, exon structure & sequences, external references and orthologues across species. zurl.co/Q5YoZ #Ensembl #Genomics #Bioinformatics
Demo: Navigating the Feature explorer app
Learn how to explore genes and transcripts using the Ensembl Feature Explorer app.In this tutorial, we use the human BRCA2 gene as an example to demonstrate ...
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Open access means faster discoveries, new ideas and scientific growth #OpenAccess #Genomics
Every rare disease diagnosis relies on open data most people never see. Our new impact report explores how Genomics England's sequencing pipeline depends on EMBL-EBI’s open data resources. 🖥️🧬 s.embl.org/EMBL-EBI-202... @genomicsengland.bsky.social @ensembl.org
Ensembl has moved! We are ahead of schedule and all sites now point to the new Ensembl at ensembl.org. It is a major milestone in our 26 year long project! 🧬🧬🧬 Refresh your browser cache for our sites if you find an error this week ⚙️
Ensembl is moving this week! 🧬 Links will point you to the new Ensembl. The default site will be ensembl.org for all species from across the tree of life. We’re starting with the Ensembl Genomes sites, and we’ll end with the Ensembl 116 site.
Explore genomes with the new Ensembl Data Platform! In this demo, see how to: Select a genome Find information about your selected genome Watch the demo and start exploring: zurl.co/qtSwQ #Ensembl #Genomics #Bioinformatics
Demo: How to select a genome in the new Ensembl data platform
Bekijk je favoriete video's, luister naar de muziek die je leuk vindt, upload originele content en deel alles met vrienden, familie en anderen op YouTube.
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Big news for European biodiversity conservation. Three major scientific communities have signed a landmark agreement through the @biogeneurope.bsky.social (BGE+) project to build a continent-wide infrastructure for biodiversity genomics. www.embl.org/news/science... #biodiversity #EUPolicy
The annual DECIPHER user survey is now available ! Please, help us to improve DECIPHER by taking 5 minutes to answer. docs.google.com/forms/d/e/1F... This is a new survey so don’t hesitate to answer it even if you had completed it last year.
We're making some changes to our new Ensembl site in the lead up to transition! Two apps have been renamed: Species selector is now Genome selector; Entity viewer is now Feature explorer. Any saved links still work - so no worries for your bookmarked genomes and genes. 🧬
NMD predictions have been updated. The first 200bp of coding nucleotides on the protein browser are now highlighted as predicted to escape the NMD - 100-200bp is shaded in light grey to reflect the evidence of gradual decrease in NMD inhibition in this region #VariantClassification
DECIPHER version 11.40 has been released. See the new features at www.deciphergenomics.org #variantinterpretation
DECIPHER v11.40: Mapping the clinical genome
DECIPHER helps the clinical community share and compare human genome variants and phenotypes in a database of tens of thousands of patients worldwide
deciphergenomics.org
Join @training.ebi.embl.org webinar on 1 July: Transitioning to the new @ensembl.org platform for genome data and annotation. We will cover features in development and the access the current Ensembl site. Register: zurl.co/VNaw3 Qs?: zurl.co/asl8M #Genomics #Bioinformatics #Training
New Ensembl FTP users, heads up! The FTP structure for the new site has been updated. The species name-based structure will be retired in August 2026. Overlap dumps are provided to help while you rework existing pipelines. Read more on our blog: zurl.co/sSbPj
We’ve updated human variant pathogenicity predictions on #Ensembl 116, which now features #AlphaMissense and #ESM1b predictors across variant and transcript views, alongside a fix to improve #REVEL score accuracy. Read more in our blog: zurl.co/EoRmm
The #Ensembl Transition webinar series starts tomorrow. If you would like to know how the transition will affect you, please join us and the @training.ebi.embl.org team! Registration for each webinar is free but essential to secure your place: www.ebi.ac.uk/training/eve...
Join our Ensembl Transition webinar series with @training.ebi.embl.org, focussing on the move to the new Ensembl browser and what it means for users.
If you teach #genomics, support #bioinf training, or use #Ensembl in your courses, check out our new Ensembl for Educators resource at zurl.co/dPKpv and read more about it on the Ensembl blog: zurl.co/rwIPx
Due to a server issue our beta.ensembl.org site is currently unable to display genome data and search queries will fail. GraphQL data cannot be served right now too. We're working to fix this as quickly as possible. Thank you for your patience. 🛠️
Visit us at #eshg2026 F4-5 at 14:00 CEST I07 Adam Frankish (Manual Genome Annotation Coordinator) and Likhitha Surapaneni, Senior Bioinformatics Developer (Ensembl Variation)
Excited to be presenting two interactive sessions at #eshg2026 in Gothenburg! 14 June, 14:00 CEST I07: UCSC & @ensembl.org Genome Browsers (F4/5) 15 June, 14:00 CEST I16: Social Media in Genetics (Sequencing Square) If you're at the meeting, come and say hello ☺️ #Genomics #HumanGenetics #SciComm
Join us at #eshg2026 for Interactive Session I07: @genomebrowser.bsky.social and @ensembl.org Browsers! Sunday, 14 June 2026 14:15-15:45 CEST Suitable for anyone with a degree-level understanding of molecular biology, bioinformatics, or genetics, and comfortable using web browsers.
DECIPHER version 11.39 has been released. See the new features at www.deciphergenomics.org #variantinterpretation
DECIPHER v11.39: Mapping the clinical genome
DECIPHER helps the clinical community share and compare human genome variants and phenotypes in a database of tens of thousands of patients worldwide
deciphergenomics.org
Ensembl 116 + Ensembl Genomes 63 are out! Explore new pig, cattle, and oat genomes, updated alignments and new VEP plugins It’s a milestone! Our last on the current platform. New data from here on is via beta.ensembl.org More info on our blog: zurl.co/MrJ2A
We're excited for our webinar tomorrow where we'll demonstrate our new Alignments viewer tool and how to explore genomic structural variants! Registration is free but essential www.ebi.ac.uk/training/eve...
The new Ensembl Alignments viewer tool for exploring genomic structural variation -
The new Ensembl Alignments viewer tool for exploring genomic structural variation -
ebi.ac.uk
Explore genomic #StructuralVariants and #GenomeAlignments in our upcoming #webinar on the new Alignments viewer in the Ensembl Data Platform. It includes a live demo comparing human reference and alternative assemblies. Registration free but essential www.ebi.ac.uk/training/eve... @ensembl.org
Explore genomic #StructuralVariants and #GenomeAlignments in our upcoming #webinar on the new Alignments viewer in the Ensembl Data Platform. It includes a live demo comparing human reference and alternative assemblies. Registration free but essential www.ebi.ac.uk/training/eve... @ensembl.org
Open genomic data powers modern life science research, and Ensembl plays a key part in this ecosystem. Developed by @ebi.embl.org we helps researchers explore genomes, variation, and comparative genomics across species. Our latest report here: zurl.co/aKKpF #Genomics #OpenScience #Bioinformatics
2026 impact report
Independent report estimates the socio-economic value of EMBL-EBI open data resources, which generate £11.8 billion annually in productivity gains delivered to a widening global user base.
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