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Nucleic Acids Research|February 25, 2025
FuSViz-visualization and interpretation of structural variation using cancer genomics and transcriptomics dataSen Zhao, Sigve Nakken, Daniel Vodak, et al.Nucleic Acids Research|July 21, 2009
The disruptive positions in human G-quadruplex motifs are less polymorphic and more conserved than their neutral counterpartsSigve Nakken, Torbjørn Rognes, Eivind HovigHuman Mutation|October 2, 2010
Impact of DNA physical properties on local sequence bias of human mutationSigve Nakken, Einar A Rødland, Eivind HovigMutation Research|March 29, 2026
Exploring Taq polymerase induced mutations in part of BRAF exon 15 by sequencing and mutation enrichmentPer O Ekstrøm, Sigve Nakken, Eivind HovigBMC Genomics|January 24, 2009
Large-scale inference of the point mutational spectrum in human segmental duplicationsSigve Nakken, Einar A Rødland, Torbjørn Rognes, et al.BMC Research Notes|November 13, 2015
Automated amplicon design suitable for analysis of DNA variants by melting techniquesPer Olaf Ekstrøm, Sigve Nakken, Morten Johansen, et al.International Journal of Cancer|July 26, 2021
Cancer Predisposition Sequencing Reporter (CPSR): A flexible variant report engine for high-throughput germline screening in cancerSigve Nakken, Vladislav Saveliev, Oliver Hofmann, et al.Bioinformatics (Oxford, England)|December 23, 2017
Personal Cancer Genome Reporter: variant interpretation report for precision oncologySigve Nakken, Ghislain Fournous, Daniel Vodák, et al.BMC Medical Genetics|February 21, 2018
Identification of genetic variants for clinical management of familial colorectal tumorsMev Dominguez-Valentin, Sigve Nakken, Hélène Tubeuf, et al.Familial Cancer|June 14, 2017
Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer familiesMev Dominguez-Valentin, Sigve Nakken, Hélène Tubeuf, et al.Pageof 55