Research Studentships | statistics
Come join us! We have an exciting PhD opportunity in statistical genetics at the University of Oxford.
More info here: bit.ly/biomedDPhil
🗓️ App deadline: June 30th 2025.
Please share!
09.06.2025 13:55 — 👍 11 🔁 8 💬 1 📌 5
SITLabs
This project was made by the new Scientific Interface & Tooling Lab (sitlabs.org) at Oxford. We will be releasing new interfaces and tools to improve scientific productivity with an initial focus on biology research.
18.12.2024 16:56 — 👍 2 🔁 0 💬 0 📌 0
Next we provided the variant mentions and paper context to gpt-4o-mini and requested structured output summarising the scientific finding. Finally we mapped all variants to the latest genome build and plotted them on our custom genome browser.
18.12.2024 16:56 — 👍 1 🔁 0 💬 1 📌 0
How to download bioRxiv on a budget
To begin we downloaded 7TB's of bioRxiv+medRxiv preprints and extracted mentions of genetic variant ID's or positions. Documented in "How to download bioRxiv on a budget": sitlabs.org/writing/bior...
18.12.2024 16:56 — 👍 1 🔁 0 💬 1 📌 0
This project started after I was trawling through Google Scholar to review a gene when I realised I had missed relevant upstream findings which hadn't been linked to the gene. I wondered if there could be a better interface to explore genetic literature?
18.12.2024 16:56 — 👍 1 🔁 0 💬 1 📌 0
Ever get lost searching through genetic literature? We've built a new interface for bioRxiv+medRxiv to directly browse preprint findings on the genome! (1/N)
Try genorxiv: sitlabs.org/genorxiv
18.12.2024 16:56 — 👍 17 🔁 7 💬 4 📌 1
nooo how am i meant to bookmark papers only to never look at them again on bsky
26.11.2024 21:44 — 👍 4 🔁 0 💬 1 📌 0
Discover the Languages of Biology
Build computational models to (help) solve biology? Join us! https://www.deboramarkslab.com
DM or mail me!
Chief Science and Strategy Officer, openRxiv. Co-Founder, bioRxiv and medRxiv.
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/
Building something valuable with a cap table I can break bread with | ex- checkout.com
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Illumina AI Lab; Previously: Rhodes Scholar, PhD at Oxford; Princeton '19 | Interested in human genetics + computational biology
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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.
DPhil student in statistical genetics @ Oxford, supervised by Cecilia Lindgren and Simon Myers. Focused on obesity and outliers. Passionate about improving global public health.
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
Assistant Investigator @ MGH / Broad / HMS. Focus on human genomics and modeling rare variation. She/her
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)
Clinical geneticist and rare disease researcher at the Broad Institute and Boston Children's Hospital
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.
DPhil Student and RA at the CRDG Lab, University of Oxford
Postdoctoral Bioinformaticial in the Computational Rare Disease Genomics group (Nicky Whiffin). univ. Oxford 🧬💻
Loves Evolution, regulation, cheese and cats. She/Her
