Philipp Rentzsch

Deciphering programs of transcriptional regulation by combined deconvolution of multiple omics layers

R. Eils, M. Schlesner, C. Herrmann, 2017, bioRxiv.

CADD: predicting the deleteriousness of variants throughout the human genome

Gregory M. Cooper, Philipp Rentzsch, Daniela Witten, 2018, Nucleic Acids Res..

ShinyButchR: Interactive NMF-based decomposition workflow of genome-scale datasets

Philipp Rentzsch, Roland Eils, Carl Herrmann, 2020, Biology methods & protocols.

CADD-Splice—improving genome-wide variant effect prediction using deep learning-derived splice scores

J. Shendure, Martin Kircher, M. Schubach, 2021, Genome Medicine.