Simon Wengert

@simon-wengert.bsky.social

Postdoc at Copenhagen University | foundation models for genomics | mtDNA heteroplasmy | ageing & psychiatric diseases

📊 My and @jhilden.bsky.social’s book has been out of print for some time, as our publisher closed down its general publishing arm. We are working on a 2nd edition, but it is not going to be ready anytime soon, so we’re making the current edition available as an e-book for €9.90. payhip.com/b/zbl43

Data visualization handbook

The Data visualization handbook by Juuso Koponen and Jonatan Hildén is a practical guide for creating compelling graphics to explain and explore data. It is primarily aimed at designers, journalists, ...

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Midway through the CSHL Symposium on AI in Biology and this far it's been a blast! Tomorrow I will be presenting our work on genomic foundation models for large-scale biomedical data analysis in poster session #3, 4:30 pm, poster #291. Come find me to connect and discuss :) #cshlsymp26

Bild

GWAS has been an incredible discovery tool for human genetics: it regularly identifies *causal* links from 1000s of SNPs to any given trait. But mechanistic interpretation is usually difficult. Our latest work on causal models for this is out yesterday: www.nature.com/articles/s41... A short🧵:

Causal modelling of gene effects from regulators to programs to traits - Nature

Approaches combining genetic association and Perturb-seq data that link genetic variants to functional programs to traits are described.

nature.com

Hiring Senior Computational Postdoc to lead large-scale scRNAseq analysis for Project JAGUAR, one of the world’s most comprehensive single-cell immune resources from Latin American ancestries. If big data, global partnerships, human diversity and immune regulation excite you, apply! bit.ly/3XyFWrW

Senior Postdoctoral Fellow

Do you want to help us improve human health and understand life on Earth? Make your mark by shaping the future to enable or deliver life-changing science to solve some of humanity’s greatest challenge...

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First time on Bsky and first big announcement! I am excited to announce that our new study explaining the missing heritability of many phenotypes using WGS data from ~347,000 UK Biobank participants has just been published in @Nature. Our manuscript is here: www.nature.com/articles/s41....

Estimation and mapping of the missing heritability of human phenotypes - Nature

WGS data were used from 347,630 individuals with European ancestry in the UK Biobank to obtain high-precision estimates of coding and non-coding rare variant heritability for 34 co...

nature.com

Postdoc opportunity! At National Genomics Infrastructure in Uppsala we're looking for a postdoc in genomics R&D. Cutting-edge methods dev in an excellent, international environment at the junction between academia and infrastructure. Deadline May 23! www.uu.se/en/about-uu/...

Postdoctoral Researcher, NGI Uppsala, SNP&SEQ Technology Platform - Uppsala University

Postdoctoral Researcher, NGI Uppsala, SNP&SEQ Technology Platform, Department of Medical Sciences, Uppsala University

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