Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Genome Medicine|August 4, 2025
varCADD: large sets of standing genetic variation enable genome-wide pathogenicity predictionLusiné Nazaretyan, Philipp Rentzsch, Martin Kircher
Biorxiv : the Preprint Server for Biology|January 23, 2024
Specifying cellular context of transcription factor regulons for exploring context-specific gene regulation programsMariia Minaeva, Júlia Domingo, Philipp Rentzsch, et al.
Genome Medicine|February 23, 2021
CADD-Splice-improving genome-wide variant effect prediction using deep learning-derived splice scoresPhilipp Rentzsch, Max Schubach, Jay Shendure, et al.
NAR Genomics and Bioinformatics|January 9, 2025
Specifying cellular context of transcription factor regulons for exploring context-specific gene regulation programsMariia Minaeva, Júlia Domingo, Philipp Rentzsch, et al.
Biorxiv : the Preprint Server for Biology|April 22, 2024
Recalibrating differential gene expression by genetic dosage variance prioritizes functionally relevant genesPhilipp Rentzsch, Aaron Kollotzek, Pejman Mohammadi, et al.
Nucleic Acids Research|October 30, 2018
CADD: predicting the deleteriousness of variants throughout the human genomePhilipp Rentzsch, Daniela Witten, Gregory M Cooper, et al.
Genome Research|September 17, 2025
Recalibrating differential gene expression by genetic dosage variance prioritizes functionally relevant genesPhilipp Rentzsch, Aaron Kollotzek, Kaushik Ram Ganapathy, et al.
Biology Methods & Protocols|December 30, 2020
ShinyButchR: Interactive NMF-based decomposition workflow of genome-scale datasetsAndres Quintero, Daniel Hübschmann, Nils Kurzawa, et al.
Scientific Reports|February 5, 2025
Whole genome sequencing in early onset advanced heart failureErik Linnér, Tomasz Czuba, Olof Gidlöf, et al.
Pageof 1