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Nucleic Acids Research|September 4, 2012
Exploring functional variant discovery in non-coding regions with SInBaDKjong-Van Lehmann, Ting ChenJournal of Computational Biology : a Journal of Computational Molecular Cell Biology|July 1, 2022
RNA Instant Quality Check: Alignment-Free RNA-Degradation DetectionKjong-van Lehmann, Andre Kahles, Magdalena Murr, et al.Bioinformatics (Oxford, England)|July 14, 2020
Mutational signature learning with supervised negative binomial non-negative matrix factorizationXinrui Lyu, Jean Garret, Gunnar Rätsch, et al.Bioinformatics (Oxford, England)|July 28, 2022
SECEDO: SNV-based subclone detection using ultra-low coverage single-cell DNA sequencingHana Rozhoňová, Daniel Danciu, Stefan Stark, et al.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|January 17, 2015
Integrative genome-wide analysis of the determinants of RNA splicing in kidney renal clear cell carcinomaKjong-Van Lehmann, André Kahles, Cyriac Kandoth, et al.Bioinformatics (Oxford, England)|December 31, 2020
SCIM: universal single-cell matching with unpaired feature setsStefan G Stark, Joanna Ficek, Francesco Locatello, et al.Nature Methods|September 28, 2023
Learning single-cell perturbation responses using neural optimal transportCharlotte Bunne, Stefan G Stark, Gabriele Gut, et al.Cancer Cell|August 7, 2018
Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 PatientsAndré Kahles, Kjong-Van Lehmann, Nora C Toussaint, et al.Bioinformatics (Oxford, England)|June 28, 2024
Probabilistic pathway-based multimodal factor analysisAlexander Immer, Stefan G Stark, Francis Jacob, et al.Genetics|May 20, 2016
Buffering of Genetic Regulatory Networks in Drosophila melanogasterJustin M Fear, Luis G León-Novelo, Alison M Morse, et al.Pageof 3