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This again: 'A simple tutorial for a complex ComplexHeatmap'. This is an end-to-end tutorial (literally, just run the code) for generating a 'ComplexHeatmap' in #R. Original paper is cell.com/cell-reports/f… #bioinformatics Centre for Translational Bioinformatics QMUL-WHRI Experimental Medicine & Rheumatology Genentech github.com/kevinblighe/E-…

Members of Centre for Translational Bioinformatics QMUL-WHRI participate in these code review sessions with the support of Queen Mary University of London ITSR team. One year of code review club with the William Harvey Research Institute | QMUL ITS Research Blog blog.hpc.qmul.ac.uk/code_review_wh…

Who wants to do a PhD in AI and Drug Discovery with Industry? 2nd March deadline! findaphd.com/phds/program/a…

@DeepMind added new proteomes to #AlphaFold database, including Leishmania infantum and T. cruzi & T. brucei, making happy the bioinformaticians who work with non-model organisms! 😌

🎉 Happy to get this out there! A new Shiny app to quickly explore hierarchical clustering by changing features, settings and annotations, evaluating them and inspecting differences. Check with install.packages("visxhclust") or at github.com/rhenkin/visxhc… #RStats

25 Lecturer/Senior Lecturer positions at Queen Mary University London, including in applications of AI in molecular and cellular biology, physiology, biomedicine, evolution, ecology. Deadline is 13 March 2022. qmul.ac.uk/sbbs/about-us/…

Diagnostics of repeat expansions has relied on targeted PCR tests. We now show that #WGS can detect pathogenic expansions at a clinical diagnostic standard. Out now The Lancet Neurology! Genomics England UCL Queen Square Institute of Neurology NHS Genomic Medicine Service Illumina Queen Mary University of London thelancet.com/journals/laneu…

Using deep learning to annotate the protein universe go.nature.com/3v4tKlv

We are hiring!!! Building on our work on short tandem repeats in the human genome, and their contribution to neurological disorders. Looking for a bioinformatician with experience in genetic analysis of mendelian & complex traits in humans. qmul.ac.uk/jobs/vacancies…

Excited by our new Drug Discovery AI PhD project, in collaboration with the Merck London Discovery Research Centre – some thoughts about how we got to this project 🧵 findaphd.com/phds/program/a…

Hey all👋, I've recently made a package called enrich-omics to directly get EnrichR and Open Targets results in Python without having to copy paste lists (that can be very error prone). Let me know what you think! Contributions and feedback welcome :) github.com/saramasarone/e…

It's #RareDiseaseDay 2022! Over 300 million people in Europe alone have a rare disease. IMPC are proud to aid the search for new cures and treatments! Find out more about how IMPC resources aid treatment and cures for rare disease using #mousemodels bit.ly/35A3AfC

On #RareDiseaseDay #RareDiseaseDay2022 delighted to be working on IMPC which is improving rare disease diagnoses, on @@EJPRareDiseases which brings together researchers across Europe, on Monarch Initiative which describes cross species phenotypes.

From the Phenogenomics group at Centre for Translational Bioinformatics QMUL-WHRI William Harvey Research Institute @DataScienceQMUL we would like to join the efforts to raise awareness of #RareDiseaseDay. We are committed and proud of our contribution to Rare Disease Research. whri-phenogenomics.github.io/whri-phenogeno…

Striking to see a gene therapy cure for a devastating and not so rare disease. Which disease is next I wonder?

Look at us, indeed! What a team! 🙌 📢Some recent efforts: * #Phenopacket schema doi.org/10.1038/s41587… * #Phenotype-driven approaches for #RareDisease #variantPrioritisation doi.org/10.1002/humu.2… * Gene discovery via mouse embryo viability screening doi.org/10.1101/2022.0…

📢Out now Genetics in Medicine our collaborative 2-cohort analysis showing evidence of UCHL1 #haploinsufficiency in #dominant #neurologic disorder with #spasticity, #ataxia, #polyneuropathy, and #opticAtrophy 👇 authors.elsevier.com/c/1fcTh3vlFUye… Fire of life Centre for Translational Bioinformatics QMUL-WHRI Genomics England #RareDisease

📢📄Check out the latest publication from #C4TB Pilar Cacheiro et al. on how information on the developmental period at which embryonic lethality occurs in the knockout mouse can inform novel #RareDisease gene discovery 👇👇👇

🙏 re-tweet or apply! 📢📢A #DataScientist/#Bioinformatician post is available within Queen Mary University of London Damian Smedley's team to work on data from the NIH - funded MorPhiC project (Molecular Phenotypes of Null Alleles in Cells) ** Deadline: 25 Nov 👇👇👇 qmul.ac.uk/jobs/vacancies…

🙏 re-tweet or apply! We are #hiring! 📢📢A 3-year Research Fellow post in #genomics is available UCL Great Ormond Street Institute of Child Health with close links with Queen Mary University of London University of Dundee to study the #genetics of #RareDisease bronchiectasis ** Deadline: 21 March 2023 👇👇👇 ucl.ac.uk/work-at-ucl/se…