Improving variant effect predictions of regulatory sequences in human disease using Machine Learning and High-throughput Assays

Zenodo (CERN European Organization for Nuclear Research) 2026 Open access

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Authors: Max Schubach
DOI: 10.5281/zenodo.18754531
Cited by: 0

Fields of Study & Subjects

Genomics and Rare Diseases Genetic Associations and Epidemiology Genomics and Chromatin Dynamics

Publication details

Journal / source
Zenodo (CERN European Organization for Nuclear Research)
Publication date
24 February 2026
Language
EN