PhD/postdoc positions available - reach out if curious about cerebellum evo-devo and autism spectrum disorders.
We’re based at Uni Tartu, Institute of Genomics (home to Estonian Biobank), and funded by @simonsfoundation.org @embo.org, and the Estonian Research Council.
PhD/postdoc positions available - reach out if curious about cerebellum evo-devo and autism spectrum disorders.
We’re based at Uni Tartu, Institute of Genomics (home to Estonian Biobank), and funded by @simonsfoundation.org @embo.org, and the Estonian Research Council.
(details below)
(details below)
https://www.biorxiv.org/content/10.64898/2026.01.20.700519v1
https://www.biorxiv.org/content/10.64898/2026.01.20.700519v1
I will miss CA deeply, but a new adventure awaits 🐟
www.nature.com/articles/d41...
I will miss CA deeply, but a new adventure awaits 🐟
www.nature.com/articles/d41...
https://www.embo.org/press-releases/ten-scientists-awarded-embo-installation-grants-2026/
#LifeSciences #research #funding
Profiling RNA and ATAC of 68k+ nuclei from 39 individuals to better understand mechanism and context for GWAS loci
We mapped the regulatory landscape of human liver at single-nucleus resolution using snMultiome, connecting genetic variants to the cell-type mechanisms underlying cardiometabolic disease.
www.sciencedirect.com/science/arti...
Profiling RNA and ATAC of 68k+ nuclei from 39 individuals to better understand mechanism and context for GWAS loci
⏰ Don’t miss it! #EMGM2026 in Davos (Switzerland) 🏔️
📅 14–15 April 2026
📝 Abstract deadline: 1 February 2026
✈️ Travel grants available
🎤 Amazing lineup of invited speakers
🔗 Details: emgm2026.sciencesconf.org
⏰ Don’t miss it! #EMGM2026 in Davos (Switzerland) 🏔️
📅 14–15 April 2026
📝 Abstract deadline: 1 February 2026
✈️ Travel grants available
🎤 Amazing lineup of invited speakers
🔗 Details: emgm2026.sciencesconf.org
aacrjournals.org/clincancerre...
aacrjournals.org/clincancerre...
Our latest work on causal models for this is out yesterday:
www.nature.com/articles/s41...
A short🧵:
Our latest work on causal models for this is out yesterday:
www.nature.com/articles/s41...
A short🧵:
We profiled ~10M PBMCs (snRNA-seq + snATAC-seq) from 1,108 Finnish donors to map how genetic variants drive complex disease through chromatin and gene regulation 🧵👇
🔗 Link: www.medrxiv.org/content/10.1...
We profiled ~10M PBMCs (snRNA-seq + snATAC-seq) from 1,108 Finnish donors to map how genetic variants drive complex disease through chromatin and gene regulation 🧵👇
🔗 Link: www.medrxiv.org/content/10.1...