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Biorxiv : the Preprint Server for Biology|May 19, 2023
Whole-genome long-read sequencing downsampling and its effect on variant calling precision and recallWilliam T Harvey, Peter Ebert, Jana Ebler, et al.Genome Research|January 8, 2024
Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recallWilliam T Harvey, Peter Ebert, Jana Ebler, et al.Nucleic Acids Research|May 15, 2010
Deep sequencing reveals differential expression of microRNAs in favorable versus unfavorable neuroblastomaJohannes H Schulte, Tobias Marschall, Marcel Martin, et al.Bioinformatics (Oxford, England)|May 17, 2015
Repeat- and error-aware comparison of deletionsRoland Wittler, Tobias Marschall, Alexander Schönhuth, et al.Nature Reviews. Genetics|July 16, 2026
Building and applying pangenome references to capture genetic diversityHufsah Ashraf, Daniel Doerr, Jana Ebler, et al.International Journal of Cancer|August 22, 2012
Next-generation RNA sequencing reveals differential expression of MYCN target genes and suggests the mTOR pathway as a promising therapy target in MYCN-amplified neuroblastomaAlexander Schramm, Johannes Köster, Tobias Marschall, et al.IEEE/ACM Transactions on Computational Biology and Bioinformatics|August 8, 2012
Probabilistic arithmetic automata and their applicationsTobias Marschall, Inke Herms, Hans-Michael Kaltenbach, et al.Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|March 12, 2020
Chromatyping: Reconstructing Nucleosome Profiles from NOMe Sequencing DataShounak Chakraborty, Stefan Canzar, Tobias Marschall, et al.Nature Genetics|April 12, 2022
Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classesJana Ebler, Peter Ebert, Wayne E Clarke, et al.Genome Biology|June 5, 2019
Haplotype-aware diplotyping from noisy long readsJana Ebler, Marina Haukness, Trevor Pesout, et al.Pageof 17