Statistical Analysis for High-Dimensional Data : The Abel Symposium 2014

por Frigessi, Arnoldo, Bühlmann, Peter, Glad, Ingrid, Langaas, Mette, Richardson, Sylvia, Vannucci, Marina
Publicado 2016

Integrated analysis of DNA-methylation and gene expression using high-dimensional penalized regression: a cohort study on bone mineral density in postmenopausal women

por Lien, Tonje G., Borgan, Ørnulf, Reppe, Sjur, Gautvik, Kaare, Glad, Ingrid Kristine
Publicado 2018

Tailored graphical lasso for data integration in gene network reconstruction

por Lingjærde, Camilla, Lien, Tonje G., Borgan, Ørnulf, Bergholtz, Helga, Glad, Ingrid K.
Publicado 2021

Estimated Comparative Integration Hotspots Identify Different Behaviors of Retroviral Gene Transfer Vectors

por Ambrosi, Alessandro, Glad, Ingrid K., Pellin, Danilo, Cattoglio, Claudia, Mavilio, Fulvio, Di Serio, Clelia, Frigessi, Arnoldo
Publicado 2011

Genome-wide estimation of transcript concentrations from spotted cDNA microarray data

por Frigessi, Arnoldo, van de Wiel, Mark A., Holden, Marit, Svendsrud, Debbie H., Glad, Ingrid K., Lyng, Heidi
Publicado 2005

Handling realistic assumptions in hypothesis testing of 3D co-localization of genomic elements

por Paulsen, Jonas, Lien, Tonje G., Sandve, Geir Kjetil, Holden, Lars, Borgan, Ørnulf, Glad, Ingrid K., Hovig, Eivind
Publicado 2013

Coordinates and intervals in graph-based reference genomes

por Rand, Knut D., Grytten, Ivar, Nederbragt, Alexander J., Storvik, Geir O., Glad, Ingrid K., Sandve, Geir K.
Publicado 2017

Graph Peak Caller: Calling ChIP-seq peaks on graph-based reference genomes

por Grytten, Ivar, Rand, Knut D., Nederbragt, Alexander J., Storvik, Geir O., Glad, Ingrid K., Sandve, Geir K.
Publicado 2019

Gene Dosage, Expression, and Ontology Analysis Identifies Driver Genes in the Carcinogenesis and Chemoradioresistance of Cervical Cancer

por Lando, Malin, Holden, Marit, Bergersen, Linn C., Svendsrud, Debbie H., Stokke, Trond, Sundfør, Kolbein, Glad, Ingrid K., Kristensen, Gunnar B., Lyng, Heidi
Publicado 2009

The Genomic HyperBrowser: inferential genomics at the sequence level

por Sandve, Geir K, Gundersen, Sveinung, Rydbeck, Halfdan, Glad, Ingrid K, Holden, Lars, Holden, Marit, Liestøl, Knut, Clancy, Trevor, Ferkingstad, Egil, Johansen, Morten, Nygaard, Vegard, Tøstesen, Eivind, Frigessi, Arnoldo, Hovig, Eivind
Publicado 2010

Validation of oligoarrays for quantitative exploration of the transcriptome

por Nygaard, Vigdis, Liu, Fang, Holden, Marit, Kuo, Winston P, Trimarchi, Jeff, Ohno-Machado, Lucila, Cepko, Connie L, Frigessi, Arnoldo, Glad, Ingrid K, Wiel, Mark A van de, Hovig, Eivind, Lyng, Heidi
Publicado 2008

The differential disease regulome

por Sandve, Geir K, Gundersen, Sveinung, Rydbeck, Halfdan, Glad, Ingrid K, Holden, Lars, Holden, Marit, Liestøl, Knut, Clancy, Trevor, Drabløs, Finn, Ferkingstad, Egil, Johansen, Morten, Nygaard, Vegard, Tøstesen, Eivind, Frigessi, Arnoldo, Hovig, Eivind
Publicado 2011

The Genomic HyperBrowser: an analysis web server for genome-scale data

por Sandve, Geir K., Gundersen, Sveinung, Johansen, Morten, Glad, Ingrid K., Gunathasan, Krishanthi, Holden, Lars, Holden, Marit, Liestøl, Knut, Nygård, Ståle, Nygaard, Vegard, Paulsen, Jonas, Rydbeck, Halfdan, Trengereid, Kai, Clancy, Trevor, Drabløs, Finn, Ferkingstad, Egil, Kalaš, Matúš, Lien, Tonje, Rye, Morten B., Frigessi, Arnoldo, Hovig, Eivind
Publicado 2013

GSuite HyperBrowser: integrative analysis of dataset collections across the genome and epigenome

por Simovski, Boris, Vodák, Daniel, Gundersen, Sveinung, Domanska, Diana, Azab, Abdulrahman, Holden, Lars, Holden, Marit, Grytten, Ivar, Rand, Knut, Drabløs, Finn, Johansen, Morten, Mora, Antonio, Lund-Andersen, Christin, Fromm, Bastian, Eskeland, Ragnhild, Gabrielsen, Odd Stokke, Ferkingstad, Egil, Nakken, Sigve, Bengtsen, Mads, Nederbragt, Alexander Johan, Thorarensen, Hildur Sif, Akse, Johannes Andreas, Glad, Ingrid, Hovig, Eivind, Sandve, Geir Kjetil
Publicado 2017