Hasil Pencarian - Stephan Ossowski

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  1. 1
    The rate and spectrum of mosaic mutations during embryogenesis revealed by RNA sequencing of 49 tissues

    The rate and spectrum of mosaic mutations during embryogenesis revealed by RNA sequencing of 49 tissues oleh Francesc Muyas, Luis Zapata, Roderic Guigó, Stephan Ossowski

    Diterbitkan 2020-05-01
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  2. 2
    Highly specific gene silencing by artificial miRNAs in rice.

    Highly specific gene silencing by artificial miRNAs in rice. oleh Norman Warthmann, Hao Chen, Stephan Ossowski, Detlef Weigel, Philippe Hervé

    Diterbitkan 2008-01-01
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  3. 3
    LOCAS--a low coverage assembly tool for resequencing projects.

    LOCAS--a low coverage assembly tool for resequencing projects. oleh Juliane D Klein, Stephan Ossowski, Korbinian Schneeberger, Detlef Weigel, Daniel H Huson

    Diterbitkan 2011-01-01
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  4. 4
    Negative selection in tumor genome evolution acts on essential cellular functions and the immunopeptidome

    Negative selection in tumor genome evolution acts on essential cellular functions and the immunopeptidome oleh Luis Zapata, Oriol Pich, Luis Serrano, Fyodor A. Kondrashov, Stephan Ossowski, Martin H. Schaefer

    Diterbitkan 2018-05-01
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  5. 5
    Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in Dystonia

    Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in Dystonia oleh Michaela Pogoda, Franz-Joachim Hilke, Franz-Joachim Hilke, Ebba Lohmann, Ebba Lohmann, Ebba Lohmann, Marc Sturm, Florian Lenz, Jakob Matthes, Francesc Muyas, Francesc Muyas, Francesc Muyas, Stephan Ossowski, Stephan Ossowski, Stephan Ossowski, Alexander Hoischen, Alexander Hoischen, Ulrike Faust, Ilnaz Sepahi, Nicolas Casadei, Nicolas Casadei, Sven Poths, Olaf Riess, Olaf Riess, Christopher Schroeder, Kathrin Grundmann

    Diterbitkan 2019-12-01
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  6. 6
    LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy

    LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy oleh Pere Soler-Palacín, Pere Soler-Palacín, Marina Garcia-Prat, Marina Garcia-Prat, Andrea Martín-Nalda, Andrea Martín-Nalda, Clara Franco-Jarava, Clara Franco-Jarava, Jacques G. Rivière, Jacques G. Rivière, Alberto Plaja, Daniela Bezdan, Daniela Bezdan, Mattia Bosio, Mattia Bosio, Mónica Martínez-Gallo, Mónica Martínez-Gallo, Stephan Ossowski, Stephan Ossowski, Stephan Ossowski, Roger Colobran, Roger Colobran, Roger Colobran

    Diterbitkan 2018-10-01
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  7. 7
    Comparative Transcriptional Profiling of Motor Neuron Disorder-Associated Genes in Various Human Cell Culture Models

    Comparative Transcriptional Profiling of Motor Neuron Disorder-Associated Genes in Various Human Cell Culture Models oleh Stefan Hauser, Stefan Hauser, Stefanie Schuster, Stefanie Schuster, Stefanie Schuster, Elena Heuten, Philip Höflinger, Philip Höflinger, Philip Höflinger, Jakob Admard, Yvonne Schelling, Yvonne Schelling, Ana Velic, Boris Macek, Stephan Ossowski, Stephan Ossowski, Ludger Schöls, Ludger Schöls, Ludger Schöls

    Diterbitkan 2020-09-01
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  8. 8
    SARS-CoV-2 infection paralyzes cytotoxic and metabolic functions of the immune cells

    SARS-CoV-2 infection paralyzes cytotoxic and metabolic functions of the immune cells oleh Yogesh Singh, Christoph Trautwein, Rolf Fendel, Naomi Krickeberg, Georgy Berezhnoy, Rosi Bissinger, Stephan Ossowski, Madhuri S. Salker, Nicolas Casadei, Olaf Riess

    Diterbitkan 2021-06-01
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  9. 9
    Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank

    Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank oleh Katherine A. Fawcett, German Demidov, Nick Shrine, Megan L. Paynton, Stephan Ossowski, Ian Sayers, Louise V. Wain, Edward J. Hollox

    Diterbitkan 2022-05-01
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  10. 10
    Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation.

    Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation. oleh Hana Susak, Laura Serra-Saurina, German Demidov, Raquel Rabionet, Laura Domènech, Mattia Bosio, Francesc Muyas, Xavier Estivill, Geòrgia Escaramís, Stephan Ossowski

    Diterbitkan 2021-02-01
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  11. 11
    Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing data

    Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing data oleh German Demidov, Joohyun Park, Sorin Armeanu‐Ebinger, Cristiana Roggia, Ulrike Faust, Isabell Cordts, Maria Blandfort, Tobias B. Haack, Christopher Schroeder, Stephan Ossowski

    Diterbitkan 2021-12-01
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  12. 12
    Genomic characterisation of clinical and environmental Pseudomonas putida group strains and determination of their role in the transfer of antimicrobial resistance genes to Pseudomonas aeruginosa

    Genomic characterisation of clinical and environmental Pseudomonas putida group strains and determination of their role in the transfer of antimicrobial resistance genes to Pseudom... oleh Silke Peter, Philipp Oberhettinger, Leonard Schuele, Ariane Dinkelacker, Wichard Vogel, Daniela Dörfel, Daniela Bezdan, Stephan Ossowski, Matthias Marschal, Jan Liese, Matthias Willmann

    Diterbitkan 2017-11-01
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  13. 13
    PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data.

    PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data. oleh Geòrgia Escaramís, Cristian Tornador, Laia Bassaganyas, Raquel Rabionet, Jose M C Tubio, Alexander Martínez-Fundichely, Mario Cáceres, Marta Gut, Stephan Ossowski, Xavier Estivill

    Diterbitkan 2013-01-01
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  14. 14
    A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ Influx.

    A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ Influx. oleh Maria Isabel Bahamonde, Selma Angèlica Serra, Oliver Drechsel, Rubayte Rahman, Anna Marcé-Grau, Marta Prieto, Stephan Ossowski, Alfons Macaya, José M Fernández-Fernández

    Diterbitkan 2015-01-01
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  15. 15
    Correction: PeSV-Fisher: Identification of Somatic and Non-Somatic Structural Variants Using Next Generation Sequencing Data.

    Correction: PeSV-Fisher: Identification of Somatic and Non-Somatic Structural Variants Using Next Generation Sequencing Data. oleh Geòrgia Escaramís, Cristian Tornador, Laia Bassaganyas, Raquel Rabionet, Jose M. C. Tubio, Alexander Martínez-Fundichely, Mario Cáceres, Marta Gut, Stephan Ossowski, Xavier Estivill

    Diterbitkan 2013-01-01
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  16. 16
    Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome

    Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome oleh Dennis Witt, Ulrike Faust, Gertrud Strobl‐Wildemann, Marc Sturm, Rebecca Buchert, Theresia Zuleger, Jakob Admard, Nicolas Casadei, Stephan Ossowski, Tobias B. Haack, Olaf Rieß, Christopher Schroeder

    Diterbitkan 2023-06-01
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  17. 17
    Nuclear gene proximity and protein interactions shape transcript covariations in mammalian single cells

    Nuclear gene proximity and protein interactions shape transcript covariations in mammalian single cells oleh Marcel Tarbier, Sebastian D. Mackowiak, João Frade, Silvina Catuara-Solarz, Inna Biryukova, Eleni Gelali, Diego Bárcena Menéndez, Luis Zapata, Stephan Ossowski, Magda Bienko, Caroline J. Gallant, Marc R. Friedländer

    Diterbitkan 2020-10-01
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  18. 18
    Genomes in clinical care

    Genomes in clinical care oleh Olaf Riess, Marc Sturm, Benita Menden, Alexandra Liebmann, German Demidov, Dennis Witt, Nicolas Casadei, Jakob Admard, Leon Schütz, Stephan Ossowski, Stacie Taylor, Sven Schaffer, Christopher Schroeder, Andreas Dufke, Tobias Haack

    Diterbitkan 2024-03-01
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  19. 19
    Tracking of Antibiotic Resistance Transfer and Rapid Plasmid Evolution in a Hospital Setting by Nanopore Sequencing

    Tracking of Antibiotic Resistance Transfer and Rapid Plasmid Evolution in a Hospital Setting by Nanopore Sequencing oleh Silke Peter, Mattia Bosio, Caspar Gross, Daniela Bezdan, Javier Gutierrez, Philipp Oberhettinger, Jan Liese, Wichard Vogel, Daniela Dörfel, Lennard Berger, Matthias Marschal, Matthias Willmann, Ivo Gut, Marta Gut, Ingo Autenrieth, Stephan Ossowski

    Diterbitkan 2020-08-01
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  20. 20
    Tracking of Antibiotic Resistance Transfer and Rapid Plasmid Evolution in a Hospital Setting by Nanopore Sequencing

    Tracking of Antibiotic Resistance Transfer and Rapid Plasmid Evolution in a Hospital Setting by Nanopore Sequencing oleh Silke Peter, Mattia Bosio, Caspar Gross, Daniela Bezdan, Javier Gutierrez, Philipp Oberhettinger, Jan Liese, Wichard Vogel, Daniela Dörfel, Lennard Berger, Matthias Marschal, Matthias Willmann, Ivo Gut, Marta Gut, Ingo Autenrieth, Stephan Ossowski

    Diterbitkan 2020-08-01
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