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Genome Biology|October 24, 2015
Teaser: Individualized benchmarking and optimization of read mapping results for NGS dataMoritz Smolka, Philipp Rescheneder, Michael C Schatz, et al.
G3 (Bethesda, Md.)|July 27, 2023
Concerning the eXclusion in human genomics: the choice of sex chromosome representation in the human genome drastically affects the number of identified variantsBrendan J Pinto, Brian O'Connor, Michael C Schatz, et al.
Computational and Structural Biotechnology Journal|December 8, 2017
LRSim: A Linked-Reads Simulator Generating Insights for Better Genome PartitioningRuibang Luo, Fritz J Sedlazeck, Charlotte A Darby, et al.
Cell Systems|January 24, 2018
Scikit-ribo Enables Accurate Estimation and Robust Modeling of Translation Dynamics at Codon ResolutionHan Fang, Yi-Fei Huang, Aditya Radhakrishnan, et al.
Nature Methods|January 19, 2023
Jasmine and Iris: population-scale structural variant comparison and analysisMelanie Kirsche, Gautam Prabhu, Rachel Sherman, et al.
Iscience|July 1, 2021
Pan-genomic matching statistics for targeted nanopore sequencingOmar Ahmed, Massimiliano Rossi, Sam Kovaka, et al.
Molecular Ecology|December 7, 2018
Genome-wide patterns of transposon proliferation in an evolutionary young hybrid fishStefan Dennenmoser, Fritz J Sedlazeck, Michael C Schatz, et al.
Genome Research|October 9, 2015
Oxford Nanopore sequencing, hybrid error correction, and de novo assembly of a eukaryotic genomeSara Goodwin, James Gurtowski, Scott Ethe-Sayers, et al.
Genome Biology|May 18, 2019
Addressing confounding artifacts in reconstruction of gene co-expression networksPrincy Parsana, Claire Ruberman, Andrew E Jaffe, et al.
Genome Biology and Evolution|April 21, 2022
Complete Sequence of a 641-kb Insertion of Mitochondrial DNA in the Arabidopsis thaliana Nuclear GenomePeter D Fields, Gus Waneka, Matthew Naish, et al.
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