Хайлтын үр дүнгүүд - Sven Rahmann

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  1. 1
    Efficient exact motif discovery

    Efficient exact motif discovery -н Tobias Marschall, Sven Rahmann

    Хэвлэсэн 2009
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    Artigo
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  2. 2
    Snakemake—a scalable bioinformatics workflow engine

    Snakemake—a scalable bioinformatics workflow engine -н Johannes Köster, Sven Rahmann

    Хэвлэсэн 2018
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    Errata/Corrigenda
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  3. 3
    HMM Logos for visualization of protein families

    HMM Logos for visualization of protein families -н Benjamin Schuster‐Böckler, Jörg Schultz, Sven Rahmann

    Хэвлэсэн 2004
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    Artigo
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  4. 4
    SimLoRD: Simulation of Long Read Data

    SimLoRD: Simulation of Long Read Data -н Bianca K. Stöcker, Johannes Köster, Sven Rahmann

    Хэвлэсэн 2016
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    Artigo
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  5. 5
    Large scale clustering of protein sequences with FORCE -A layout based heuristic for weighted cluster editing

    Large scale clustering of protein sequences with FORCE -A layout based heuristic for weighted cluster editing -н Tobias Wittkop, Jan Baumbach, Francisco Pereira Lobo, Sven Rahmann

    Хэвлэсэн 2007
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    Artigo
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  6. 6
    N6-Adenosine Methylation in MiRNAs

    N6-Adenosine Methylation in MiRNAs -н Tea Berulava, Sven Rahmann, Katrin Rademacher, L. Klein‐Hitpass, Bernhard Horsthemke

    Хэвлэсэн 2015
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    Artigo
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  7. 7
    Optimal robust non-unique probe selection using Integer Linear Programming

    Optimal robust non-unique probe selection using Integer Linear Programming -н Gunnar W. Klau, Sven Rahmann, Alexander Schliep, Martin Vingron, Knut Reinert

    Хэвлэсэн 2004
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    Artigo
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  8. 8
    Discovering motifs that induce sequencing errors

    Discovering motifs that induce sequencing errors -н Manuel Allhoff, Alexander Schönhuth, Marcel Martin, Ivan G. Costa, Sven Rahmann, Tobias Marschall

    Хэвлэсэн 2013
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    Artigo
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  9. 9
    Non-responsiveness to cardioprotection by ischaemic preconditioning in Ossabaw minipigs with genetic predisposition to, but without the phenotype of the metabolic syndrome

    Non-responsiveness to cardioprotection by ischaemic preconditioning in Ossabaw minipigs with genetic predisposition to, but without the phenotype of the metabolic syndrome -н Petra Kleinbongard, Helmut Raphael Lieder, Andreas Skyschally, Mouhamad Alloosh, Axel Gödecke, Sven Rahmann, Michael Sturek, Gerd Heusch

    Хэвлэсэн 2022
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    Carta
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  10. 10
    Comprehensive transcriptome analysis provides new insights into nutritional strategies and phylogenetic relationships of chrysophytes

    Comprehensive transcriptome analysis provides new insights into nutritional strategies and phylogenetic relationships of chrysophytes -н Daniela Beißer, Nadine Graupner, Christina Böck, Sabina Wodniok, Lars Großmann, Matthijs Vos, Bernd Sures, Sven Rahmann, Jens Boenigk

    Хэвлэсэн 2017
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    Artigo
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  11. 11
    Deep sequencing reveals differential expression of microRNAs in favorable versus unfavorable neuroblastoma

    Deep sequencing reveals differential expression of microRNAs in favorable versus unfavorable neuroblastoma -н Johannes H. Schulte, Tobias Marschall, Marcel Martin, Philip Rosenstiel, Pieter Mestdagh, Stefanie Schlierf, Theresa Thor, Jo Vandesompele, Angelika Eggert, Stefan Schreiber, Sven Rahmann, Alexander Schramm

    Хэвлэсэн 2010
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    Artigo
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  12. 12
    Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

    Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3 -н Marcel Martin, Lars Maßhöfer, Petra Temming, Sven Rahmann, Claudia H.D. Metz, Norbert Bornfeld, Johannes van de Nes, Ludger Klein‐Hitpaß, Alan G. Hinnebusch, Bernhard Horsthemke, Dietmar Lohmann, Michael Zeschnigk

    Хэвлэсэн 2013
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    Artigo
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  13. 13
    Human <scp>TLR</scp> 8 senses <scp>UR</scp> / <scp>URR</scp> motifs in bacterial and mitochondrial <scp>RNA</scp>

    Human <scp>TLR</scp> 8 senses <scp>UR</scp> / <scp>URR</scp> motifs in bacterial and mitochondrial <scp>RNA</scp> -н Anne Krüger, Marina Oldenburg, Chiranjeevi Chebrolu, Daniela Beißer, Julia Kolter, Anna M. Sigmund, Jörg Steinmann, Simon Schäfer, Hubertus Hochrein, Sven Rahmann, Hermann Wagner, Philipp Henneke, Veit Hornung, Jan Buer, Carsten J. Kirschning

    Хэвлэсэн 2015
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    Artigo
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  14. 14
    A germ cell‐specific ageing pattern in otherwise healthy men

    A germ cell‐specific ageing pattern in otherwise healthy men -н Sandra Laurentino, Jann‐Frederik Cremers, Bernhard Horsthemke, Frank Tüttelmann, K. Czeloth, Michael Zitzmann, Eva Pohl, Sven Rahmann, Christopher Schröder, Sven Berres, K. Redmαnn, Claudia Krallmann, Stefan Schlatt, Sabine Kliesch, Jörg Gromoll

    Хэвлэсэн 2020
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    Artigo
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  15. 15
    CDKN2A deletion in supratentorial ependymoma with RELA alteration indicates a dismal prognosis: a retrospective analysis of the HIT ependymoma trial cohort

    CDKN2A deletion in supratentorial ependymoma with RELA alteration indicates a dismal prognosis: a retrospective analysis of the HIT ependymoma trial cohort -н Stephanie T. Jünger, Felipe Andreiuolo, Martin Mynarek, Inken Wohlers, Sven Rahmann, Ludger Klein‐Hitpaß, Evelyn Dörner, Anja zur Mühlen, Natalia Velez-Char, Katja von Hoff, Monika Warmuth‐Metz, Rolf‐Dieter Kortmann, Beate Timmermann, André O. von Bueren, Stefan Rutkowski, Torsten Pietsch

    Хэвлэсэн 2020
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    Artigo
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  16. 16
    Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylation

    Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylation -н Laura Godfrey, Jan Förster, Sven‐Thorsten Liffers, Christopher Schröder, Johannes Köster, Leonie Henschel, Kerstin U. Ludwig, David Lähnemann, Marija Trajkovic‐Arsic, Diana Behrens, Aldo Scarpa, Rita T. Lawlor, Kathrin E. Witzke, Barbara Sitek, Steven A. Johnsen, Sven Rahmann, Bernhard Horsthemke, Michael Zeschnigk, Jens T. Siveke

    Хэвлэсэн 2024
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    Artigo
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  17. 17
    Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations

    Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations -н Claudia Voigt, André Mégarbané, Kornelia Neveling, Johanna Christina Czeschik, Beate Albrecht, Bert Callewaert, Florian von Deimling, Andreas Hehr, Marie Falkenberg Smeland, Rainer König, Alma Kuechler, Carlo Marcelis, Maria Puiu, William Reardon, Hilde Monica Frostad Riise Stensland, Bernd Schweiger, Marloes Steehouwer, Christopher Teller, Marcel Martin, Sven Rahmann, Ute Hehr, Han G. Brunner, Hermann‐Josef Lüdecke, Dagmar Wieczorek

    Хэвлэсэн 2013
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    Artigo
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  18. 18
    Epigenetic dynamics of monocyte-to-macrophage differentiation

    Epigenetic dynamics of monocyte-to-macrophage differentiation -н Stefan Wallner, Christopher Schröder, Elsa Leitão, Tea Berulava, Claudia Haak, Daniela Beißer, Sven Rahmann, Andreas S. Richter, Thomas Manke, Ulrike Bönisch, Laura Arrigoni, Sebastian Fröhler, Filippos Klironomos, Wei Chen, Nikolaus Rajewsky, Fabian Müller, Peter Ebert, Thomas Lengauer, Matthias Barann, Philip Rosenstiel, Gilles Gasparoni, Karl Nordström, Jörn Walter, Benedikt Brors, Gideon Zipprich, Bärbel Felder, Ludger Klein‐Hitpaß, Corinna Attenberger, Gerd Schmitz, Bernhard Horsthemke

    Хэвлэсэн 2016
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    Artigo
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  19. 19
    A mechanistic classification of clinical phenotypes in neuroblastoma

    A mechanistic classification of clinical phenotypes in neuroblastoma -н Sandra Ackermann, Maria Cartolano, Barbara Hero, Anne Welte, Yvonne Kahlert, Andrea Roderwieser, Christoph Bartenhagen, Esther Walter, Judith Gecht, Laura Kerschke, Ruth Volland, Roopika Menon, Johannes M. Heuckmann, Moritz Gartlgruber, Sabine Hartlieb, Kai‐Oliver Henrich, Konstantin Okonechnikov, Janine Altmüller, Peter Nürnberg, Steve Lefever, Bram De Wilde, Frederik Sand, Fakhera Ikram, Carolina Rosswog, J. Fischer, Jessica Theißen, Falk Hertwig, Aatur D. Singhi, Thorsten Simon, Wenzel Vogel, Sven Perner, Barbara Krug, Matthias Schmidt, Sven Rahmann, Viktor Achter, Ulrich Lang, Christian Vokuhl, Monika Ortmann, Reinhard Büttner, Angelika Eggert, Frank Speleman, Roderick J. O’Sullivan, Roman K. Thomas, Frank Berthold, Jo Vandesompele, Alexander Schramm, Frank Westermann, Johannes H. Schulte, Martin Peifer, Matthias Fischer

    Хэвлэсэн 2018
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    Artigo
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  20. 20
    A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling

    A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling -н Dagmar Wieczorek, Nina Bögershausen, Filippo Beleggia, Sabine Steiner-Haldenstätt, Esther Pohl, Yun Li, Esther Milz, Marcel Martin, Holger Thiele, Janine Altmüller, Yasemin Alanay, Hülya Kayserili, Ludger Klein‐Hitpaß, Stefan Böhringer, Andreas Wollstein, Beate Albrecht, Koray Boduroğlu, Almuth Caliebe, Krystyńa Chrzańowska, Özgür Çoğulu, Francesca Cristofoli, Johanna Christina Czeschik, Koenraad Devriendt, Maria Teresa Dotti, Nursel Elçioğlu, Blanca Gener, Timm O. Goecke, Małgorzata Krajewska‐Walasek, Encarna Guillén‐Navarro, Joussef Hayek, Gunnar Houge, Esra KAYA KILIÇ, Pelin Özlem Şimşek‐Kiper, Vanesa López‐González, Alma Kuechler, Stanislas Lyonnet, Francesca Mari, Annabella Marozza, Michèle Mathieu Dramard, Barbara Mikat, G Morin, Fanny Morice‐Picard, Ferda Özkınay, Anita Rauch, Alessandra Renieri, Sigrid Tinschert, Gülen Eda Ütine, Catheline Vilain, Rossella Vivarelli, Christiane Zweier, Peter Nürnberg, Sven Rahmann, Joris Vermeesch, Hermann‐Josef Lüdecke, Michael Zeschnigk, Bernd Wollnik

    Хэвлэсэн 2013
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    Artigo
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