Amazon Web Services in action

por Wittig, Michael, Wittig, Andreas
Publicado 2016

Amazon Web Services in action

por Wittig, Michael, Wittig, Andreas
Publicado 2019

CNVineta: a data mining tool for large case–control copy number variation datasets

por Wittig, Michael, Helbig, Ingo, Schreiber, Stefan, Franke, Andre
Publicado 2010

Fitness consequences of polymorphic inversions in the zebra finch genome

por Knief, Ulrich, Hemmrich-Stanisak, Georg, Wittig, Michael, Franke, Andre, Griffith, Simon C., Kempenaers, Bart, Forstmeier, Wolfgang
Publicado 2016

The age related markers lipofuscin and apoptosis show different genetic architecture by QTL mapping in short-lived Nothobranchius fish

por Ng'oma, Enoch, Reichwald, Kathrin, Dorn, Alexander, Wittig, Michael, Balschun, Tobias, Franke, Andre, Platzer, Matthias, Cellerino, Allesandro
Publicado 2014

Efficacy assessment of SNP sets for genome-wide disease association studies

por Wollstein, Andreas, Herrmann, Alexander, Wittig, Michael, Nothnagel, Michael, Franke, Andre, Nürnberg, Peter, Schreiber, Stefan, Krawczak, Michael, Hampe, Jochen
Publicado 2007

Acute physical exercise improves shifting in adolescents at school: evidence for a dopaminergic contribution

por Berse, Timo, Rolfes, Kathrin, Barenberg, Jonathan, Dutke, Stephan, Kuhlenbäumer, Gregor, Völker, Klaus, Winter, Bernward, Wittig, Michael, Knecht, Stefan
Publicado 2015

A post-GWAS analysis of predicted regulatory variants and tuberculosis susceptibility

por Uren, Caitlin, Henn, Brenna M., Franke, Andre, Wittig, Michael, van Helden, Paul D., Hoal, Eileen G., Möller, Marlo
Publicado 2017

A tissue-specific landscape of sense/antisense transcription in the mouse intestine

por Klostermeier, Ulrich C, Barann, Matthias, Wittig, Michael, Häsler, Robert, Franke, Andre, Gavrilova, Olga, Kreck, Benjamin, Sina, Christian, Schilhabel, Markus B, Schreiber, Stefan, Rosenstiel, Philip
Publicado 2011

Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci

por Saadati, Hamid Reza, Wittig, Michael, Helbig, Ingo, Häsler, Robert, Anderson, Carl A., Mathew, Christopher G., Kupcinskas, Limas, Parkes, Miles, Karlsen, Tom Hemming, Rosenstiel, Philip, Schreiber, Stefan, Franke, Andre
Publicado 2016

High-throughput method for the hybridisation-based targeted enrichment of long genomic fragments for PacBio third-generation sequencing

por Steiert, Tim Alexander, Fuß, Janina, Juzenas, Simonas, Wittig, Michael, Hoeppner, Marc Patrick, Vollstedt, Melanie, Varkalaite, Greta, ElAbd, Hesham, Brockmann, Christian, Görg, Siegfried, Gassner, Christoph, Forster, Michael, Franke, Andre
Publicado 2022

Development of a high-resolution NGS-based HLA-typing and analysis pipeline

por Wittig, Michael, Anmarkrud, Jarl A., Kässens, Jan C., Koch, Simon, Forster, Michael, Ellinghaus, Eva, Hov, Johannes R., Sauer, Sascha, Schimmler, Manfred, Ziemann, Malte, Görg, Siegfried, Jacob, Frank, Karlsen, Tom H., Franke, Andre
Publicado 2015

Complement Receptor 1 (CR1, CD35) Polymorphisms and Soluble CR1: A Proposed Anti-inflammatory Role to Quench the Fire of “Fogo Selvagem” Pemphigus Foliaceus

por Oliveira, Luana Caroline, Kretzschmar, Gabriela Canalli, dos Santos, Andressa Cristina Moraes, Camargo, Carolina Maciel, Nisihara, Renato Mitsunori, Farias, Ticiana Della Justina, Franke, Andre, Wittig, Michael, Schmidt, Enno, Busch, Hauke, Petzl-Erler, Maria Luiza, Boldt, Angelica Beate Winter
Publicado 2019

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 2013

Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome

por Helbig, Ingo, Barcia, Giulia, Pendziwiat, Manuela, Ganesan, Shiva, Mueller, Stefanie H., Helbig, Katherine L., Vaidiswaran, Priya, Xian, Julie, Galer, Peter D., Afawi, Zaid, Specchio, Nicola, Kluger, Gerhard, Kuhlenbäumer, Gregor, Appenzeller, Silke, Wittig, Michael, Kramer, Uri, van Baalen, Andreas, Nabbout, Rima
Publicado 2020

Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants

por Gueuning, Morgan, Thun, Gian Andri, Wittig, Michael, Galati, Anna-Lena, Meyer, Stefan, Trost, Nadine, Gourri, Elise, Fuss, Janina, Sigurdardottir, Sonja, Merki, Yvonne, Neuenschwander, Kathrin, Busch, Yannik, Trojok, Peter, Schäfer, Marco, Gottschalk, Jochen, Franke, Andre, Gassner, Christoph, Peter, Wolfgang, Frey, Beat M., Mattle-Greminger, Maja P.
Publicado 2022

Validity and Prognostic Value of a Polygenic Risk Score for Parkinson’s Disease

por Koch, Sebastian, Laabs, Björn-Hergen, Kasten, Meike, Vollstedt, Eva-Juliane, Becktepe, Jos, Brüggemann, Norbert, Franke, Andre, Krämer, Ulrike M., Kuhlenbäumer, Gregor, Lieb, Wolfgang, Mollenhauer, Brit, Neis, Miriam, Trenkwalder, Claudia, Schäffer, Eva, Usnich, Tatiana, Wittig, Michael, Klein, Christine, König, Inke R., Lohmann, Katja, Krawczak, Michael, Caliebe, Amke
Publicado 2021

Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans

por Krause-Kyora, Ben, Nutsua, Marcel, Boehme, Lisa, Pierini, Federica, Pedersen, Dorthe Dangvard, Kornell, Sabin-Christin, Drichel, Dmitriy, Bonazzi, Marion, Möbus, Lena, Tarp, Peter, Susat, Julian, Bosse, Esther, Willburger, Beatrix, Schmidt, Alexander H., Sauter, Jürgen, Franke, Andre, Wittig, Michael, Caliebe, Amke, Nothnagel, Michael, Schreiber, Stefan, Boldsen, Jesper L., Lenz, Tobias L., Nebel, Almut
Publicado 2018

Systematic Association Mapping Identifies NELL1 as a Novel IBD Disease Gene

por Franke, Andre, Hampe, Jochen, Rosenstiel, Philip, Becker, Christian, Wagner, Florian, Häsler, Robert, Little, Randall D., Huse, Klaus, Ruether, Andreas, Balschun, Tobias, Wittig, Michael, ElSharawy, Abdou, Mayr, Gabriele, Albrecht, Mario, Prescott, Natalie J., Onnie, Clive M., Fournier, Hélène, Keith, Tim, Radelof, Uwe, Platzer, Matthias, Mathew, Christopher G., Stoll, Monika, Krawczak, Michael, Nürnberg, Peter, Schreiber, Stefan
Publicado 2007

Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine mapping in the MHC and genome wide

por Stuart, Philip E., Tsoi, Lam C., Nair, Rajan P., Ghosh, Manju, Kabra, Madhulika, Shaiq, Pakeeza A., Raja, Ghazala K., Qamar, Raheel, Thelma, B.K., Patrick, Matthew T., Parihar, Anita, Singh, Sonam, Khandpur, Sujay, Kumar, Uma, Wittig, Michael, Degenhardt, Frauke, Tejasvi, Trilokraj, Voorhees, John J., Weidinger, Stephan, Franke, Andre, Abecasis, Goncalo R., Sharma, Vinod K., Elder, James T.
Publicado 2021