We’re recruiting for multiple positions in my lab in New York and Stockholm, at MSc and PhD levels. If you’re interested in pursuing creative systems genetics questions with tools/data like Developmental GTEx, CRISPR and single-cell, please read further / share. 1/

Kudos again to the team Gabriel M. C. Longo, Sergi Sayols, Diana Kotini, belilab, protein production and genomics IMB facilities Islamabad Metblogs SFB 1361 - DNA Repair and Genome Stability

I am so very proud of ⁦Charlie Bell⁩ and this manuscript from ⁦The Dawson Lab⁩ ⁦Peter Mac Research⁩ - A labour of love driven by curiosity, resilience and incredible teamwork over many years. We hope it contributes substantially to our field nature.com/articles/s4158…

Just published in PLOS Genetics. Luciana Gómez Acuña @EliasFriman Ilya Flyamer 💙💛 show surprising differences in what 3C- and imaging-based methods tell us about enhancer-promoter communication. MRC_HGU Institute of Genetics and Cancer journals.plos.org/plosgenetics/a… ed.ac.uk/institute-gene…

Diverse and interdisciplinary projects suitable to many backgrounds, in projects that develop skills important for the future of biomedical sciences. If you are interested in protein structure prediction, DNA and disease, please get in touch with myself or Joe Marsh

Introducing scE2G: a new model to link enhancers to target genes using single-cell data. Excited that scE2G will enable building enhancer maps in hundreds of cell types in the human body! Wonderful collaboration with Robin Andersson Wei-Lin Qiu maya sheth and others 👇

In our latest study with Joe Marsh, we extend our work on phenotype-level molecular mechanism prediction. Read more here: biorxiv.org/content/10.110…

New paper out in Genome Biology! 🎉 We lay out best-practice guidelines for releasing variant effect predictors, developed through the Atlas of Variant Effects Alliance Atlas of Variant Effects Alliance Open, interpretable, and clinically useful VEPs are the goal. 📄 doi.org/10.1186/s13059…

Genetic variants🧬 can cause protein-coding mutations resulting in disease. What about in alternative isoforms? Excited to share my 1st first-author pre-print! Here we show many variants reside in tissue-specific isoforms, causing coding mutations. A🧵 1/ biorxiv.org/content/10.110…