@richardsever.bsky.social
Co-Founder, bioRxiv and medRxiv. Assistant Director, Cold Spring Harbor Laboratory Press.
@benlehner.bsky.social
Solve Biology Head of Generative Genomics, Wellcome Sanger Institute, Cambridge, UK Systems + Synthetic Biology, CRG, Barcelona http://barcelonacollaboratorium.com http://allox.bio https://www.sanger.ac.uk/programme/generative-and-synthetic-genomics/
@rowans.me
left http://Checkout.com to build AI copilot for renters, now building for real estate pros https://using.casa
@bioinfomatt.bsky.social
Director, Clinical Bioinformatics Software at Oxford Nanopore in the EPI2ME team. Interested in regulated application of Nanopore sequencing. Also bikes, beers, trains, and the American Office.
@astheeggeggs.bsky.social
Senior statistical geneticist in the Lindgren Lab at the Big Data Institute in Oxford
@samvidav.bsky.social
Schmidt AI in Science postdoc at Oxford; Rhodes Scholar, Princeton '19; Bangalore | Human genetics + computational biology
@ceclindgren.bsky.social
Co-Founder and Chief Scientist | Venture Partner | Professor | Mentor | Proud mom of 3 ✨
@ewanbirney.bsky.social
Executive Director EMBL. I have an insatiable love of biology. Consultant to ONT and Cantata (Dovetail)
@cpmoxford.bsky.social
The Centre for Personalised Medicine (CPM) is a partnership between the University of Oxford’s Centre for Human Genetics and St Anne’s College. We provide a focus for multidisciplinary communication, engagement and research.
@nbaya.bsky.social
DPhil student in statistical genetics @ Oxford, supervised by Cecilia Lindgren and Simon Myers. Focused on obesity and outliers. Passionate about improving global public health.
@aaronquinlan.bsky.social
Origins and consequences of genome mutation; software for genomic discovery. Prof. and Chair of Human Genetics at U. of Utah. https://www.genetics.utah.edu/ http://quinlanlab.org
@ksamocha.bsky.social
Assistant Investigator @ MGH / Broad / HMS. Focus on human genomics and modeling rare variation. She/her
@hdashnow.bsky.social
Asst. Prof, CU Biomedical Informatics. #RareDisease #Genomics #STRs #bioinformatics #WomenInSTEM. Parent. Aussie. she/her Views my own. https://dashnowlab.org/ Img by familydestinationsguide (CC-BY)
@anneotation.bsky.social
Clinical geneticist and rare disease researcher at the Broad Institute and Boston Children's Hospital
@rbeagrie.bsky.social
Group leader and Wellcome Sir Henry Dale Fellow based at the Centre for Human Genetics at Oxford University. Interested in genomics, single-cell technologies, 3D DNA folding and chromatin disruption in human disease. He/him.
@alextremophile.bsky.social
Postdoctoral Bioinformaticial in the Computational Rare Disease Genomics group (Nicky Whiffin). univ. Oxford 🧬💻 Loves Evolution, regulation, cheese and cats. She/Her
@hkilpinen.bsky.social
Assistant Professor in Genome Biology @HiLIFE_helsinki, @FIMM_UH, @UH_Neuro and @BioEnvHelsinki. Stem cells, single cells, genomics, and neurodevelopment.
@mehurles.bsky.social
Director, Wellcome Sanger Institute. Decipherer of developmental disorders. Co-founder Congenica. Dad, husband, cyclist, gardener. Views own.
@philippamay.bsky.social
Consultant Clinical Scientist in Genomics. Talk to me about paediatric cancer, cardiovascular and respiratory disease, telomeres..... Veggie Londoner with a fondness for Ireland, halloumi, chocolate orange Twirls and wildlife. Easily startled.
@rachelbuc.bsky.social
Cardiovascular genetic scientist, crafter, mum. Passionate about opening up cardiovascular research to more people - @thehearthive.bsky.social. Has too many hobbies. London, UK
@drjennylord.bsky.social
Lecturer in Systems Biology at the University of Sheffield. Interested in bioinformatics, RNA, splicing, big data, rare disease diagnostics and neuroscience. Also dogs.
@agoriely.bsky.social
Human genetics, rare disease and de novo variant detection | selfish selection | mosaicism | cell competition | paternal age effects | spermatogenesis | testis @University of Oxford @MRC- WIMM
@chundru.bsky.social
Postdoc University of Exeter 🇮🇪🇮🇳🇬🇧 Integrating 'omics data into rare variant genetic analyses Formerly at Sanger institute working on recessive developmental disorders in DDD
@emiliewigdor.bsky.social
Postdoc in neurogenetics | Sanders Lab at University of Oxford and IDRM | JRF at the Centre for Personalised Medicine
@htanudisastro.bsky.social
MD-PhD candidate at the University of Sydney & Garvan Institute. Studying tandem repeats in single-cell contexts w/ @dgmacarthur.bsky.social
@carolinefwright.bsky.social
Academic research scientist in human genetics and genomic medicine; pianist & composer; hiker & outdoors enthusiast.
@christeldepienne.bsky.social
Molecular geneticist | Neurogenetics | repeat expansions | chromosome X | snRNAs | and more
@poseypod.bsky.social
Physician-scientist, Adult genetics, Human genetics research, Baylor College of Medicine. Thoughts expressed = my own.
@eedhaene.bsky.social
postdoc @ http://debaerelab.com @ https://fungenlab-ugent.be | 3D genome, gene regulation, structural variation | retina, neurodev, space!
@gc4gc.bsky.social
rare disease geneticist | epilepsy | epigenetics | iPSCs | mentor & genetics MedEd | immigrant | tweets about science, lab fun & occasionally our tiny hooman https://sites.northwestern.edu/carvilllab/
@jonnyfrazer.bsky.social
Probabilistic machine learning to address questions in evolution and health #EvolutionaryMedicine. PI at the Centre for Genomic Regulation, co-leading a group with Mafalda Dias. Previously Harvard.
@danrdanny.bsky.social
CODA. Dad. Interested in genetics, long-read sequencing, and ultramarathon running. Assistant Professor at University of Washington. The command line is my happy place. https://millerlaboratory.com
@rich-genomics.bsky.social
CEO @GenomicsEngland, Honorary Consultant and Associate Professor in Clinical Genetics @GOSH. Still just about a runner
@polona.bsky.social
DVM PhD | Researcher at the University of Auckland | Genomics, variant interpretation | Rare diseases | Cancer, Molecular Tumour Boards | Inherited cardiac diseases | 🧬
@ruebenadawes.bsky.social
Sydney girl, Fulbright recipient 2020-2021 with Monkol Lek. PhD Kids Research Sydney 2022, now postdoc with @nickywhiffin.bsky.social at BDI Oxford. Splicing & smORFs!
@inaklockner.bsky.social
Postdoc exploring new gene editing therapies for the neurodevelopmental disorder #AngelmanSyndrome at #UNCZylkaLab, also interested in post-transcriptional gene regulation via non-coding RNAs in neuromuscular disease |she/her|🇩🇪 🇺🇲
@heidirehm.bsky.social
Genomic medicine researcher; chief genomics officer at MGH; clinical lab director at @broadinstitute
@jkpritch.bsky.social
My lab at Stanford studies human population genetics and complex traits.
@robert.bio
Co-founder at https://omgenomics.com. Creator of https://42basepairs.com, https://sandbox.bio, https://biowasm.com, https://levelupwasm.com. Bioinformatics, genomics. About me: https://robert.bio
@chloeterwagne.bsky.social
Computational Biology PhD Candidate @TheCrick and @UCL | 💻 Machine Learning | 🧬 Functional Genomics | 🚀 Exploring Coding & Non-coding
@owlposting1.bsky.social
ml eng at dyno therapeutics. i write about bio/ml at http://owlposting.com
@yun-s-song.bsky.social
Professor of EECS and Statistics at UC Berkeley. Mathematical and computational biologist.
@sirodoht.bsky.social
https://shoshincollege.org / https://laniakeabooks.org / https://mataroa.blog
@doctorveera.bsky.social
MBBS, MD, PhD | GWAS storyteller | Scientist at Regeneron | Human genetics & drug discovery in Neuroscience & Psychiatry
@nickywhiffin.bsky.social
Associate Professor @ Big Data Institute, University of Oxford 2024 Lister Institute Fellow genomics | rare disease | gene regulation | genetic therapies https://rarediseasegenomics.org/ (field) hockey player | cyclist | hiker