't Hart LM

Discovery of drug-omics associations in type 2 diabetes with generative deep-learning models.

Allesøe RL, Lundgaard AT, Hernández Medina R, ..., Brunak S, IMI DIRECT Consortium

Nat. Biotechnol. - (-) - [2023-01-02; online 2023-01-02]

Affinity Proteomics Stockholm [Collaborative]

A saturated map of common genetic variants associated with human height.

Yengo L, Vedantam S, Marouli E, ..., Visscher PM, Hirschhorn JN

Nature 610 (7933) 704-712 [2022-10-00; online 2022-10-12]

NGI SNP genotyping [Service] NGI Uppsala (SNP&SEQ Technology Platform) [Service] National Genomics Infrastructure [Service]

Predicting and elucidating the etiology of fatty liver disease: A machine learning modeling and validation study in the IMI DIRECT cohorts.

Atabaki-Pasdar N, Ohlsson M, Viñuela A, ..., Pavo I, Franks PW

PLoS Med. 17 (6) e1003149 [2020-06-00; online 2020-06-19]

Affinity Proteomics Stockholm [Collaborative]

Rare and low-frequency coding variants alter human adult height.

Marouli E, Graff M, Medina-Gomez C, ..., Deloukas P, Lettre G

Nature 542 (7640) 186-190 [2017-02-09; online 2017-02-01]

Bioinformatics Support for Computational Resources [Service] NGI Uppsala (SNP&SEQ Technology Platform) [Service] National Genomics Infrastructure [Service]