Kornel Labun
Stilling
Forsker
Tilhørighet
Publikasjoner
Vitenskapelig artikkel
- Tilahun Bizuayehu, Teshome; Labun, Kornel; Jakubec, Martin et al. (2022). Long-read single-molecule RNA structure sequencing using nanopore. (ekstern lenke)
- Tjeldnes, Håkon; Labun, Kornel; Torres Cleuren, Yamila Nicole et al. (2021). ORFik: a comprehensive R toolkit for the analysis of translation. (ekstern lenke)
- Reint, Ganna; Li, Zhuokun; Labun, Kornel et al. (2021). Rapid genome editing by CRISPR-Cas9-POLD3 fusion. (ekstern lenke)
- Labun, Kornel; Krause, Maximilian; Torres Cleuren, Yamila Nicole et al. (2021). CRISPR Genome Editing Made Easy Through the CHOPCHOP Website. (ekstern lenke)
- Chyzynska, Katarzyna; Labun, Kornel; Jones, Carl Matthew et al. (2021). Deep conservation of ribosome stall sites across RNA processing genes. (ekstern lenke)
- Krause, Maximilian; Niazi, Adnan Muhammad; Labun, Kornel et al. (2019). tailfindr: Alignment-free poly(A) length measurement for Oxford Nanopore RNA and DNA sequencing. (ekstern lenke)
- Labun, Kornel; Montague, Tessa G.; Krause, Maximilian et al. (2019). CHOPCHOP v3: expanding the CRISPR web toolbox beyond genome editing. (ekstern lenke)
- Labun, Kornel; Guo, Xiaoge; Chavez, Alejandro et al. (2019). Accurate analysis of genuine CRISPR editing events with ampliCan. (ekstern lenke)
- Valen, Eivind; Labun, Kornel; Montague, Tessa G. et al. (2016). CHOPCHOP v2: a web tool for the next generation of CRISPR genome engineering. (ekstern lenke)
- Stokowy, Tomasz; Garbulowski, Mateusz; Fiskerstrand, Torunn et al. (2016). RareVariantVis: New tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data. (ekstern lenke)