RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data. - Tomasz Stokowy; Mateusz Garbulowski; Torunn Fiskerstrand; Rita Holdhus; Kornel Labun; Pawel Sztromwasser; Christian Gilissen; Alexander Hoischen; Gunnar Houge; Kjell Petersen; Inge Jonassen; Vidar M. Steen (Bioinform., 2016)

CHOPCHOP v2: a web tool for the next generation of CRISPR genome engineering. - Kornel Labun; Tessa G. Montague; James A. Gagnon; Summer B. Thyme; Eivind Valen (Nucleic Acids Res., 2016)

CHOPCHOP v3: expanding the CRISPR web toolbox beyond genome editing. - Kornel Labun; Tessa G. Montague; Maximilian Krause; Yamila N. Torres cleuren; Håkon Tjeldnes; Eivind Valen (Nucleic Acids Res., 2019)

ORFik: a comprehensive R toolkit for the analysis of translation. - Håkon Tjeldnes; Kornel Labun; Yamila N. Torres cleuren; Katarzyna Chyzynska; Michal Swirski; Eivind Valen (BMC Bioinform., 2021)