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Nucleic Acids Research|July 18, 2006
Kalign, Kalignvu and Mumsa: web servers for multiple sequence alignmentTimo Lassmann, Erik L L SonnhammerStem Cell Research & Therapy|February 10, 2022
CRISPR single base editing, neuronal disease modelling and functional genomics for genetic variant analysis: pipeline validation using Kleefstra syndrome EHMT1 haploinsufficiencyVanessa S Fear, Catherine A Forbes, Denise Anderson, et al.FEBS Letters|October 2, 2002
Quality assessment of multiple alignment programsTimo Lassmann, Erik L L SonnhammerBMC Bioinformatics|December 14, 2005
Kalign--an accurate and fast multiple sequence alignment algorithmTimo Lassmann, Erik L L SonnhammerBioinformatics (Oxford, England)|September 10, 2009
TagDust--a program to eliminate artifacts from next generation sequencing dataTimo Lassmann, Yoshihide Hayashizaki, Carsten O DaubBioinformatics (Oxford, England)|November 20, 2010
SAMStat: monitoring biases in next generation sequencing dataTimo Lassmann, Yoshihide Hayashizaki, Carsten O DaubGene|February 17, 2022
Functional validation of variants of unknown significance using CRISPR gene editing and transcriptomics: A Kleefstra syndrome case studyVanessa S Fear, Catherine A Forbes, Denise Anderson, et al.Nucleic Acids Research|December 24, 2008
Kalign2: high-performance multiple alignment of protein and nucleotide sequences allowing external featuresTimo Lassmann, Oliver Frings, Erik L L SonnhammerNAR Genomics and Bioinformatics|December 20, 2024
Mining single-cell data for cell type-disease associationsKevin G Chen, Kathryn O Farley, Timo LassmannNature Protocols|February 25, 2012
5' end-centered expression profiling using cap-analysis gene expression and next-generation sequencingHazuki Takahashi, Timo Lassmann, Mitsuyoshi Murata, et al.Pageof 17