A method to build extended sequence context models of point mutations and indels

por Bethune, Jörn, Kleppe, April, Besenbacher, Søren
Publicado 2022

Whole genome association mapping by incompatibilities and local perfect phylogenies

por Mailund, Thomas, Besenbacher, Søren, Schierup, Mikkel H
Publicado 2006

A fast algorithm for genome-wide haplotype pattern mining

por Besenbacher, Søren, Pedersen, Christian NS, Mailund, Thomas
Publicado 2009

Identifying disease associated genes by network propagation

por Qian, Yu, Besenbacher, Søren, Mailund, Thomas, Schierup, Mikkel Heide
Publicado 2014

Prediction of Primary Tumors in Cancers of Unknown Primary

por Søndergaard, Dan, Nielsen, Svend, Pedersen, Christian N.S., Besenbacher, Søren
Publicado 2017

Hierarchical Classification of Cancers of Unknown Primary Using Multi-Omics Data

por Bavafaye Haghighi, Elham, Knudsen, Michael, Elmedal Laursen, Britt, Besenbacher, Søren
Publicado 2019

Studying mutation rate evolution in primates—a need for systematic comparison of computational pipelines

por Bergeron, Lucie A, Besenbacher, Søren, Schierup, Mikkel H, Zhang, Guojie
Publicado 2021

Assembly and analysis of 100 full MHC haplotypes from the Danish population

por Jensen, Jacob M., Villesen, Palle, Friborg, Rune M., Mailund, Thomas, Besenbacher, Søren, Schierup, Mikkel H.
Publicado 2017

Pathway Analysis of Skin from Psoriasis Patients after Adalimumab Treatment Reveals New Early Events in the Anti-Inflammatory Mechanism of Anti-TNF-α

por Langkilde, Ane, Olsen, Lene C., Sætrom, Pål, Drabløs, Finn, Besenbacher, Søren, Raaby, Line, Johansen, Claus, Iversen, Lars
Publicado 2016

A site specific model and analysis of the neutral somatic mutation rate in whole-genome cancer data

por Bertl, Johanna, Guo, Qianyun, Juul, Malene, Besenbacher, Søren, Nielsen, Morten Muhlig, Hornshøj, Henrik, Pedersen, Jakob Skou, Hobolth, Asger
Publicado 2018

Unsupervised detection of fragment length signatures of circulating tumor DNA using non-negative matrix factorization

por Renaud, Gabriel, Nørgaard, Maibritt, Lindberg, Johan, Grönberg, Henrik, De Laere, Bram, Jensen, Jørgen Bjerggaard, Borre, Michael, Andersen, Claus Lindbjerg, Sørensen, Karina Dalsgaard, Maretty, Lasse, Besenbacher, Søren
Publicado 2022

The germline mutational process in rhesus macaque and its implications for phylogenetic dating

por Bergeron, Lucie A, Besenbacher, Søren, Bakker, Jaco, Zheng, Jiao, Li, Panyi, Pacheco, George, Sinding, Mikkel-Holger S, Kamilari, Maria, Gilbert, M Thomas P, Schierup, Mikkel H, Zhang, Guojie
Publicado 2021

Multi-nucleotide de novo Mutations in Humans

por Besenbacher, Søren, Sulem, Patrick, Helgason, Agnar, Helgason, Hannes, Kristjansson, Helgi, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Magnusson, Olafur Th., Thorsteinsdottir, Unnur, Masson, Gisli, Kong, Augustine, Gudbjartsson, Daniel F., Stefansson, Kari
Publicado 2016

Variation and association to diabetes in 2000 full mtDNA sequences mined from an exome study in a Danish population

por Li, Shengting, Besenbacher, Soren, Li, Yingrui, Kristiansen, Karsten, Grarup, Niels, Albrechtsen, Anders, Sparsø, Thomas, Korneliussen, Thorfinn, Hansen, Torben, Wang, Jun, Nielsen, Rasmus, Pedersen, Oluf, Bolund, Lars, Schierup, Mikkel H
Publicado 2014

Evolution of the germline mutation rate across vertebrates

por Bergeron, Lucie A., Besenbacher, Søren, Zheng, Jiao, Li, Panyi, Bertelsen, Mads Frost, Quintard, Benoit, Hoffman, Joseph I., Li, Zhipeng, St. Leger, Judy, Shao, Changwei, Stiller, Josefin, Gilbert, M. Thomas P., Schierup, Mikkel H., Zhang, Guojie
Publicado 2023

Rate of de novo mutations, father’s age, and disease risk

por Kong, Augustine, Frigge, Michael L., Masson, Gisli, Besenbacher, Soren, Sulem, Patrick, Magnusson, Gisli, Gudjonsson, Sigurjon A., Sigurdsson, Asgeir, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Wong, Wendy, Sigurdsson, Gunnar, Walters, G. Bragi, Steinberg, Stacy, Helgason, Hannes, Thorleifsson, Gudmar, Gudbjartsson, Daniel F., Helgason, Agnar, Magnusson, Olafur Th., Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado 2012

The Mutationathon highlights the importance of reaching standardization in estimates of pedigree-based germline mutation rates

por Bergeron, Lucie A, Besenbacher, Søren, Turner, Tychele, Versoza, Cyril J, Wang, Richard J, Price, Alivia Lee, Armstrong, Ellie, Riera, Meritxell, Carlson, Jedidiah, Chen, Hwei-yen, Hahn, Matthew W, Harris, Kelley, Kleppe, April Snøfrid, López-Nandam, Elora H, Moorjani, Priya, Pfeifer, Susanne P, Tiley, George P, Yoder, Anne D, Zhang, Guojie, Schierup, Mikkel H
Publicado 2022

Whole genome characterization of sequence diversity of 15,220 Icelanders

por Jónsson, Hákon, Sulem, Patrick, Kehr, Birte, Kristmundsdottir, Snaedis, Zink, Florian, Hjartarson, Eirikur, Hardarson, Marteinn T., Hjorleifsson, Kristjan E., Eggertsson, Hannes P., Gudjonsson, Sigurjon Axel, Ward, Lucas D., Arnadottir, Gudny A., Helgason, Einar A., Helgason, Hannes, Gylfason, Arnaldur, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Rafnar, Thorunn, Besenbacher, Soren, Frigge, Michael L., Stacey, Simon N., Magnusson, Olafur Th., Thorsteinsdottir, Unnur, Masson, Gisli, Kong, Augustine, Halldorsson, Bjarni V., Helgason, Agnar, Gudbjartsson, Daniel F., Stefansson, Kari
Publicado 2017

Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios

por Besenbacher, Søren, Liu, Siyang, Izarzugaza, José M. G., Grove, Jakob, Belling, Kirstine, Bork-Jensen, Jette, Huang, Shujia, Als, Thomas D., Li, Shengting, Yadav, Rachita, Rubio-García, Arcadio, Lescai, Francesco, Demontis, Ditte, Rao, Junhua, Ye, Weijian, Mailund, Thomas, Friborg, Rune M., Pedersen, Christian N. S., Xu, Ruiqi, Sun, Jihua, Liu, Hao, Wang, Ou, Cheng, Xiaofang, Flores, David, Rydza, Emil, Rapacki, Kristoffer, Damm Sørensen, John, Chmura, Piotr, Westergaard, David, Dworzynski, Piotr, Sørensen, Thorkild I. A., Lund, Ole, Hansen, Torben, Xu, Xun, Li, Ning, Bolund, Lars, Pedersen, Oluf, Eiberg, Hans, Krogh, Anders, Børglum, Anders D., Brunak, Søren, Kristiansen, Karsten, Schierup, Mikkel H., Wang, Jun, Gupta, Ramneek, Villesen, Palle, Rasmussen, Simon
Publicado 2015

Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus

por Stacey, Simon N., Sulem, Patrick, Zanon, Carlo, Gudjonsson, Sigurjon A., Thorleifsson, Gudmar, Helgason, Agnar, Jonasdottir, Aslaug, Besenbacher, Soren, Kostic, Jelena P., Fackenthal, James D., Huo, Dezheng, Adebamowo, Clement, Ogundiran, Temidayo, Olson, Janet E., Fredericksen, Zachary S., Wang, Xianshu, Look, Maxime P., Sieuwerts, Anieta M., Martens, John W. M., Pajares, Isabel, Garcia-Prats, Maria D., Ramon-Cajal, Jose M., de Juan, Ana, Panadero, Angeles, Ortega, Eugenia, Aben, Katja K. H., Vermeulen, Sita H., Asadzadeh, Fatemeh, van Engelenburg, K. C. Anton, Margolin, Sara, Shen, Chen-Yang, Wu, Pei-Ei, Försti, Asta, Lenner, Per, Henriksson, Roger, Johansson, Robert, Enquist, Kerstin, Hallmans, Göran, Jonsson, Thorvaldur, Sigurdsson, Helgi, Alexiusdottir, Kristin, Gudmundsson, Julius, Sigurdsson, Asgeir, Frigge, Michael L., Gudmundsson, Larus, Kristjansson, Kristleifur, Halldorsson, Bjarni V., Styrkarsdottir, Unnur, Gulcher, Jeffrey R., Hemminki, Kari, Lindblom, Annika, Kiemeney, Lambertus A., Mayordomo, Jose I., Foekens, John A., Couch, Fergus J., Olopade, Olufunmilayo I., Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Rafnar, Thorunn, Johannsson, Oskar T., Stefansson, Kari
Publicado 2010