GrabBlur - a framework to facilitate the secure exchange of whole-exome and -genome SNV data using VCF files

Por Stade, Björn, Seelow, Dominik, Thomsen, Ingo, Krawczak, Michael, Franke, Andre
Publicado em 2014

Whole genome and exome sequencing of monozygotic twins discordant for Crohn’s disease

Por Petersen, Britt-Sabina, Spehlmann, Martina E, Raedler, Andreas, Stade, Björn, Thomsen, Ingo, Rabionet, Raquel, Rosenstiel, Philip, Schreiber, Stefan, Franke, Andre
Publicado em 2014

Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing

Por ElSharawy Abdou, Forster Michael, Schracke Nadine, Keller Andreas, Thomsen Ingo, Petersen Britt-Sabina, Stade Björn, Stähler Peer, Schreiber Stefan, Rosenstiel Philip, Franke Andre
Publicado em 2012-08-01

Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing

Por ElSharawy, Abdou, Forster, Michael, Schracke, Nadine, Keller, Andreas, Thomsen, Ingo, Petersen, Britt-Sabina, Stade, Björn, Stähler, Peer, Schreiber, Stefan, Rosenstiel, Philip, Franke, Andre
Publicado em 2012

Early-onset Crohn’s disease and autoimmunity associated with a variant in CTLA-4

Por Zeissig, Sebastian, Petersen, Britt-Sabina, Tomczak, Michal, Melum, Espen, Huc-Claustre, Emilie, Dougan, Stephanie K, Laerdahl, Jon K, Stade, Björn, Forster, Michael, Schreiber, Stefan, Weir, Dascha, Leichtner, Alan M, Franke, Andre, Blumberg, Richard S
Publicado no Gut (2014)

From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software

Por Forster, Michael, Forster, Peter, Elsharawy, Abdou, Hemmrich, Georg, Kreck, Benjamin, Wittig, Michael, Thomsen, Ingo, Stade, Björn, Barann, Matthias, Ellinghaus, David, Petersen, Britt-Sabina, May, Sandra, Melum, Espen, Schilhabel, Markus B., Keller, Andreas, Schreiber, Stefan, Rosenstiel, Philip, Franke, Andre
Publicado em 2013

Association Between Variants of PRDM1 and NDP52 and Crohn’s Disease, Based on Exome Sequencing and Functional Studies

Por Ellinghaus, David, Zhang, Hu, Zeissig, Sebastian, Lipinski, Simone, Till, Andreas, Jiang, Tao, Stade, Björn, Bromberg, Yana, Ellinghaus, Eva, Keller, Andreas, Rivas, Manuel A, Skieceviciene, Jurgita, Doncheva, Nadezhda T, Liu, Xiao, Liu, Qing, Jiang, Fuman, Forster, Michael, Mayr, Gabriele, Albrecht, Mario, Häsler, Robert, Boehm, Bernhard O, Goodall, Jane, Berzuini, Carlo R, Lee, James, Andersen, Vibeke, Vogel, Ulla, Kupcinskas, Limas, Kayser, Manfred, Krawczak, Michael, Nikolaus, Susanna, Weersma, Rinse K, Ponsioen, Cyriel Y, Sans, Miquel, Wijmenga, Cisca, Strachan, David P, McArdle, Wendy L, Vermeire, Séverine, Rutgeerts, Paul, Sanderson, Jeremy D, Mathew, Christopher G, Vatn, Morten H, Wang, Jun, Nöthen, Markus M, Duerr, Richard H, Büning, Carsten, Brand, Stephan, Glas, Jürgen, Winkelmann, Juliane, Illig, Thomas, Latiano, Anna, Annese, Vito, Halfvarson, Jonas, D’Amato, Mauro, Daly, Mark J, Nothnagel, Michael, Karlsen, Tom H, Subramani, Suresh, Rosenstiel, Philip, Schreiber, Stefan, Parkes, Miles, Franke, Andre
Publicado em 2013

Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options

Por Fischer, Ute, Forster, Michael, Rinaldi, Anna, Risch, Thomas, Sungalee, Stéphanie, Warnatz, Hans-Jörg, Bornhauser, Beat, Gombert, Michael, Kratsch, Christina, Stütz, Adrian M., Sultan, Marc, Tchinda, Joelle, Worth, Catherine L., Amstislavskiy, Vyacheslav, Badarinarayan, Nandini, Baruchel, André, Bartram, Thies, Basso, Giuseppe, Canpolat, Cengiz, Cario, Gunnar, Cavé, Hélène, Dakaj, Dardane, Delorenzi, Mauro, Dobay, Maria Pamela, Eckert, Cornelia, Ellinghaus, Eva, Eugster, Sabrina, Frismantas, Viktoras, Ginzel, Sebastian, Haas, Oskar A., Heidenreich, Olaf, Hemmrich-Stanisak, Georg, Hezaveh, Kebria, Höll, Jessica I., Hornhardt, Sabine, Husemann, Peter, Kachroo, Priyadarshini, Kratz, Christian P., te Kronnie, Geertruy, Marovca, Blerim, Niggli, Felix, McHardy, Alice C., Moorman, Anthony V., Panzer-Grümayer, Renate, Petersen, Britt S., Raeder, Benjamin, Ralser, Meryem, Rosenstiel, Philip, Schäfer, Daniel, Schrappe, Martin, Schreiber, Stefan, Schütte, Moritz, Stade, Björn, Thiele, Ralf, von der Weid, Nicolas, Vora, Ajay, Zaliova, Marketa, Zhang, Langhui, Zichner, Thomas, Zimmermann, Martin, Lehrach, Hans, Borkhardt, Arndt, Bourquin, Jean-Pierre, Franke, Andre, Korbel, Jan O., Stanulla, Martin, Yaspo, Marie-Laure
Publicado no Nat Genet (2015)