If you are interested in biodiversity and would like to talk about potential informatics services that would contribute to resources such as @GBIF or @MGnifyDB please reach out to me.
If you are interested in biodiversity and would like to talk about potential informatics services that would contribute to resources such as @GBIF or @MGnifyDB please reach out to me.
Very pleased to see that @ensembl is this week's featured GCBR. A good time to also point towards our latest developments too such as https://t.co/OET9tNU4qR.
Our featured GCBR of the Week is @ensembl , a genome browser for vertebrate genomes that supports research in comparative genomics, evolution, sequence variation and transcriptional regulation.
Click the link to find out more : https://t.co/XNLrr3e3nS
@wellcometrust@UKRI_News@EU_Commission@EMBL@NIH @SavetheTasmanianDevil
#globalbiodata
#openscience
Our featured GCBR of the Week is @ensembl , a genome browser for vertebrate genomes that supports research in comparative genomics, evolution, sequence variation and transcriptional regulation.
Click the link to find out more : https://t.co/XNLrr3e3nS
@wellcometrust@UKRI_News@EU_Commission@EMBL@NIH @SavetheTasmanianDevil
#globalbiodata
#openscience
Join the @GA4GH in leading our product management and development. A massive opportunity to shape the future of standards development amongst other things.
🚀 Join EMBL-EBI as a Product Management Lead for GA4GH. Collaborate with global leaders in genomics and healthcare to set international standards. Apply now and make an impact! #Genomics#TechJobs#EMBLEBI
https://t.co/f9hv2yYVg4
🚀 Join EMBL-EBI as a Product Management Lead for GA4GH. Collaborate with global leaders in genomics and healthcare to set international standards. Apply now and make an impact! #Genomics#TechJobs#EMBLEBI
https://t.co/f9hv2yYVg4
Last year, @deciphergenomic made the move over to EMBL-EBI after many successful years at @sangerinstitute and this year DECIPHER celebrates its 20th anniversary 🎉
Find out more about DECIPHER and the move over to EMBL-EBI.
https://t.co/rAexalOn6P
This #RareDiseaseDay we’re shining the spotlight on @deciphergenomic, our database for genetic and phenotypic data which helps further our understanding of rare diseases and improving patient diagnoses.
Find out more 👇
https://t.co/prCRIbbG5p
Save the Date! The 2024 Curating the Clinical Genome scientific conference will be held in Baltimore, Maryland May 9-10, 2024. CCG24 is co-hosted by ClinGen and @decipher_wtsi. Registration and Call for Abstracts will open in January. https://t.co/6044e4qaSb
Thrilled to announce that @VdaGeraldine is joining the community team @SeqeraLabs 🎉 Already well known to the community through her work with #GATK and #WDL, we're excited to see what insights and experience she can bring to the @nextflowio world!
https://t.co/eJeceLSoro
📢 @GoogleDeepMind’s new AI tool, #AlphaMissense, has catalogued 89% of all 71 million possible missense #variants, predicting their potential to cause disease 🧬 Best part? It is freely available and now integrated as an #Ensembl#VEP plugin! 🥳
➡️ https://t.co/JNoSY0yy4c
AlphaMissense from @GoogleDeepMind is already available via @Ensembl VEP as a plugin. Another example of an excellent collaboration between them and @emblebi building the previous successes of AlphaFold. Great work by the Ensembl team especially our variation resources
The new AlphaMissense catalogue from @GoogleDeepMind can be used with the @ensembl Variant Effect Predictor to predict variant pathogenicity and therefore aid interpretation.
https://t.co/AMAnSs9ScW
This has been a long road since our PR was opened 4th March 2020. I am immensely proud of the work that's gone into refget from its origins in the CRAM Reference Registry to now as a foundational standard in genomics. Thank you to all who have contributed
It's official: #refget v2.0 is the next GA4GH standard. https://t.co/srAPlu4Biu
This API for reliably finding the right reference sequence powers all #CRAM files. v2.0 users include GA4GH VRS, @ENASequence, and soon @ensembl.
Thanks to @emblebi's @tcezard & @enscore and the team!
A huge amount of work has gone into making the move from the Wellcome Sanger Institute to EMBL-EBI. We are proud to have such a powerful and well used service now part of our portfolio. Congratulations to all at EMBL and Sanger who made this possible.
The DECIPHER project is joining EMBL-EBI!
DECIPHER is a powerful data resource for the diagnosis and discovery of rare diseases. By moving to EMBL-EBI, the project will develop through support from our data management experts.
https://t.co/rAexalOn6P
All of the pangenomes are available for access through our Rapid Release @ensembl portal including T2T (https://t.co/1G2dsSbiLG). We are all exceptionally proud at Ensembl to be part of this new phase of global efforts to better understand human diversity
Genomes differ slightly among individuals and so using one standard reference genome has limitations.
Researchers from @HumanPangenome have released a more complete collection of genome sequences – the human pangenome – to better capture human diversity.
https://t.co/weDMhOLXCm