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Nucleic Acids Research
|
July 21, 2009
The disruptive positions in human G-quadruplex motifs are less polymorphic and more conserved than their neutral counterparts
Sigve Nakken, Torbjørn Rognes, Eivind Hovig
Mutation Research
|
March 29, 2026
Exploring Taq polymerase induced mutations in part of BRAF exon 15 by sequencing and mutation enrichment
Per O Ekstrøm, Sigve Nakken, Eivind Hovig
Human Mutation
|
October 2, 2010
Impact of DNA physical properties on local sequence bias of human mutation
Sigve Nakken, Einar A Rødland, Eivind Hovig
Nucleic Acids Research
|
February 25, 2025
FuSViz-visualization and interpretation of structural variation using cancer genomics and transcriptomics data
Sen Zhao, Sigve Nakken, Daniel Vodak, et al.
BMC Research Notes
|
November 13, 2015
Automated amplicon design suitable for analysis of DNA variants by melting techniques
Per Olaf Ekstrøm, Sigve Nakken, Morten Johansen, et al.
BMC Genomics
|
January 24, 2009
Large-scale inference of the point mutational spectrum in human segmental duplications
Sigve Nakken, Einar A Rødland, Torbjørn Rognes, 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 cancer
Sigve Nakken, Vladislav Saveliev, Oliver Hofmann, et al.
Journal of Molecular Evolution
|
March 10, 2010
Unstable DNA repair genes shaped by their own sequence modifying phenotypes
Daniel S Falster, Sigve Nakken, Marie Bergem-Ohr, et al.
Bioinformatics (Oxford, England)
|
December 23, 2017
Personal Cancer Genome Reporter: variant interpretation report for precision oncology
Sigve Nakken, Ghislain Fournous, Daniel Vodák, et al.
Fertility and Sterility
|
January 29, 2016
Sequencing of FTO and ALKBH5 in men undergoing infertility work-up identifies an infertility-associated variant and two missense mutations
Miriam Landfors, Sigve Nakken, Markus Fusser, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 61) with videos related to
Sort By:
Page
of 7
Nucleic Acids Research
|
July 21, 2009
The disruptive positions in human G-quadruplex motifs are less polymorphic and more conserved than their neutral counterparts
Sigve Nakken, Torbjørn Rognes, Eivind Hovig
Mutation Research
|
March 29, 2026
Exploring Taq polymerase induced mutations in part of BRAF exon 15 by sequencing and mutation enrichment
Per O Ekstrøm, Sigve Nakken, Eivind Hovig
Human Mutation
|
October 2, 2010
Impact of DNA physical properties on local sequence bias of human mutation
Sigve Nakken, Einar A Rødland, Eivind Hovig
Nucleic Acids Research
|
February 25, 2025
FuSViz-visualization and interpretation of structural variation using cancer genomics and transcriptomics data
Sen Zhao, Sigve Nakken, Daniel Vodak, et al.
BMC Research Notes
|
November 13, 2015
Automated amplicon design suitable for analysis of DNA variants by melting techniques
Per Olaf Ekstrøm, Sigve Nakken, Morten Johansen, et al.
BMC Genomics
|
January 24, 2009
Large-scale inference of the point mutational spectrum in human segmental duplications
Sigve Nakken, Einar A Rødland, Torbjørn Rognes, 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 cancer
Sigve Nakken, Vladislav Saveliev, Oliver Hofmann, et al.
Journal of Molecular Evolution
|
March 10, 2010
Unstable DNA repair genes shaped by their own sequence modifying phenotypes
Daniel S Falster, Sigve Nakken, Marie Bergem-Ohr, et al.
Bioinformatics (Oxford, England)
|
December 23, 2017
Personal Cancer Genome Reporter: variant interpretation report for precision oncology
Sigve Nakken, Ghislain Fournous, Daniel Vodák, et al.
Fertility and Sterility
|
January 29, 2016
Sequencing of FTO and ALKBH5 in men undergoing infertility work-up identifies an infertility-associated variant and two missense mutations
Miriam Landfors, Sigve Nakken, Markus Fusser, et al.
Page
of 7