Options available for profiling small samples: a review of sample amplification technology when combined with microarray profiling

por Nygaard, Vigdis, Hovig, Eivind
Publicado em 2006

Differential Protein Network Analysis of the Immune Cell Lineage

por Clancy, Trevor, Hovig, Eivind
Publicado em 2014

Profiling networks of distinct immune-cells in tumors

por Clancy, Trevor, Hovig, Eivind
Publicado no BMC Bioinformatics (2016)

The BRCA2 variant c.68-7 T>A is associated with breast cancer

por Møller, Pål, Hovig, Eivind
Publicado no Hered Cancer Clin Pract (2017)

Retraction Note to: The BRCA2 variant c.68–7 T > A is associated with breast cancer

por Møller, Pål, Hovig, Eivind
Publicado no Hered Cancer Clin Pract (2018)

Our genes, our selves: hereditary breast cancer and biological citizenship in Norway

por Møller, Pål, Hovig, Eivind
Publicado no Med Health Care Philos (2017)

The disruptive positions in human G-quadruplex motifs are less polymorphic and more conserved than their neutral counterparts

por Nakken, Sigve, Rognes, Torbjørn, Hovig, Eivind
Publicado em 2009

Stitchprofiles.uio.no: analysis of partly melted DNA conformations using stitch profiles

por Tøstesen, Eivind, Jerstad, Geir Ivar, Hovig, Eivind
Publicado em 2005

Methods that remove batch effects while retaining group differences may lead to exaggerated confidence in downstream analyses

por Nygaard, Vegard, Rødland, Einar Andreas, Hovig, Eivind
Publicado no Biostatistics (2016)

Large-scale inference of the point mutational spectrum in human segmental duplications

por Nakken, Sigve, Rødland, Einar A, Rognes, Torbjørn, Hovig, Eivind
Publicado em 2009

The mathematics of tanning

por Thingnes, Josef, Øyehaug, Leiv, Hovig, Eivind, Omholt, Stig W
Publicado em 2009

Predicting Physical Interactions between Protein Complexes

por Clancy, Trevor, Rødland, Einar Andreas, Nygard, Ståle, Hovig, Eivind
Publicado em 2013

Ten Simple Rules for Reproducible Computational Research

por Sandve, Geir Kjetil, Nekrutenko, Anton, Taylor, James, Hovig, Eivind
Publicado em 2013

Automated amplicon design suitable for analysis of DNA variants by melting techniques

por Ekstrøm, Per Olaf, Nakken, Sigve, Johansen, Morten, Hovig, Eivind
Publicado no BMC Res Notes (2015)

Genome build information is an essential part of genomic track files

por Kanduri, Chakravarthi, Domanska, Diana, Hovig, Eivind, Sandve, Geir Kjetil
Publicado no Genome Biol (2017)

Understanding the Melanocyte Distribution in Human Epidermis: An Agent-Based Computational Model Approach

por Thingnes, Josef, Lavelle, Timothy J., Hovig, Eivind, Omholt, Stig W.
Publicado em 2012

Melanoma brain colonization involves the emergence of a brain-adaptive phenotype

por Nygaard, Vigdis, Prasmickaite, Lina, Vasiliauskaite, Kotryna, Clancy, Trevor, Hovig, Eivind
Publicado no Oncoscience (2014)

Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift

por Møller, Pål, Dominguez-Valentin, Mev, Rødland, Einar Andreas, Hovig, Eivind
Publicado no Cancers (Basel) (2019)

Correction: Møller, P.; et al. Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. Cancers 2019, 11...

por Møller, Pål, Dominguez-Valentin, Mev, Rødland, Einar Andreas, Hovig, Eivind
Publicado no Cancers (Basel) (2020)

Accuracy and efficiency of germline variant calling pipelines for human genome data

por Zhao, Sen, Agafonov, Oleg, Azab, Abdulrahman, Stokowy, Tomasz, Hovig, Eivind
Publicado no Sci Rep (2020)