Resultados de búsqueda - Marcel Martin

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  1. 1
    Cutadapt removes adapter sequences from high-throughput sequencing reads

    Cutadapt removes adapter sequences from high-throughput sequencing reads por Marcel Martin

    Publicado 2011
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  2. 2
    Read-Based Phasing and Analysis of Phased Variants with WhatsHap

    Read-Based Phasing and Analysis of Phased Variants with WhatsHap por Marcel Martin, Peter Ebert, Tobias Marschall

    Publicado 2022
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  3. 3
    Atropos: specific, sensitive, and speedy trimming of sequencing reads

    Atropos: specific, sensitive, and speedy trimming of sequencing reads por John P. Didion, Marcel Martin, Francis S. Collins

    Publicado 2017
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  4. 4
    Discovering motifs that induce sequencing errors

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

    Publicado 2013
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  5. 5
    WhatsHap: fast and accurate read-based phasing

    WhatsHap: fast and accurate read-based phasing por Marcel Martin, Murray Patterson, Shilpa Garg, Sarah O. Fischer, Nadia Pisanti, Gunnar W. Klau, Alexander Schöenhuth, Tobias Marschall

    Publicado 2016
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  6. 6
    High-Quality Library Preparation for NGS-Based Immunoglobulin Germline Gene Inference and Repertoire Expression Analysis

    High-Quality Library Preparation for NGS-Based Immunoglobulin Germline Gene Inference and Repertoire Expression Analysis por Néstor Vázquez Bernat, Martin Corcoran, Uta Hardt, Mateusz Kaduk, Ganesh E. Phad, Marcel Martin, Gunilla B. Karlsson Hedestam

    Publicado 2019
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  7. 7
    Clonal relations in the mouse brain revealed by single-cell and spatial transcriptomics

    Clonal relations in the mouse brain revealed by single-cell and spatial transcriptomics por Michael Ratz, Leonie von Berlin, Ludvig Larsson, Marcel Martin, Jakub Orzechowski Westholm, Gioele La Manno, Joakim Lundeberg, Jonas Frisén

    Publicado 2022
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  8. 8
    Production of individualized V gene databases reveals high levels of immunoglobulin genetic diversity

    Production of individualized V gene databases reveals high levels of immunoglobulin genetic diversity por Martin Corcoran, Ganesh E. Phad, Néstor Vázquez Bernat, Christiane Stahl‐Hennig, Noriyuki Sumida, Mats A. A. Persson, Marcel Martin, Gunilla B. Karlsson Hedestam

    Publicado 2016
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  9. 9
    Head-to-Head Comparison between [68Ga]Ga-DOTA.SA.FAPi and [18F]F-FDG PET/CT Imaging in Patients with Breast Cancer

    Head-to-Head Comparison between [68Ga]Ga-DOTA.SA.FAPi and [18F]F-FDG PET/CT Imaging in Patients with Breast Cancer por Sanjana Ballal, Madhav Prasad Yadav, Frank Roesch, Nicky Wakade, Shobhana Raju, Parvind Sheokand, Prashant Mishra, Euy Sung Moon, Madhavi Tripathi, Marcel Martin, Chandrasekhar Bal

    Publicado 2023
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  10. 10
    Improved FAPI-radiopharmaceutical pharmacokinetics from the perspectives of a dose escalation study

    Improved FAPI-radiopharmaceutical pharmacokinetics from the perspectives of a dose escalation study por Adrianna Bilinska, Sanjana Ballal, Chandrasekhar Bal, Tilman Läppchen, Eirinaios Pilatis, Elena Arias Menéndez, Euy Sung Moon, Marcel Martin, Frank Rösch, Axel Rominger, Eleni Gourni

    Publicado 2025
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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 por 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

    Publicado 2010
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  12. 12
    De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data

    De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data por Adam Ameur, Huiwen Che, Marcel Martin, Ignas Bunikis, Johan Dahlberg, Ida Höijer, Susana Häggqvist, Francesco Vezzi, Jessica Nordlund, Pall I. Olason, Lars Feuk, Ulf Gyllensten

    Publicado 2018
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  13. 13
    Novel Generation of FAP Inhibitor-Based Homodimers for Improved Application in Radiotheranostics

    Novel Generation of FAP Inhibitor-Based Homodimers for Improved Application in Radiotheranostics por Marcel Martin, Sanjana Ballal, Madhav Prasad Yadav, Chandrasekhar Bal, Yentl Van Rymenant, Joni De Loose, Emile Verhulst, Ingrid De Meester, Pieter Van der Veken, Frank Roesch

    Publicado 2023
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  14. 14
    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 por 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

    Publicado 2013
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  15. 15
    Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants

    Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants por M. Garcia, Szilveszter Juhos, Malin Larsson, Pall I. Olason, Marcel Martin, Jesper Eisfeldt, Sebastian DiLorenzo, Johanna Sandgren, Teresita Díaz de Ståhl, Philip Ewels, Valtteri Wirta, Monica Nistér, Max Käller, Björn Nystedt

    Publicado 2020
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  16. 16
    Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants

    Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants por M. Garcia, Szilveszter Juhos, Malin Larsson, Pall I. Olason, Marcel Martin, Jesper Eisfeldt, Sebastian DiLorenzo, Johanna Sandgren, Teresita Díaz de Ståhl, Philip Ewels, Valtteri Wirta, Monica Nistér, Max Käller, Björn Nystedt

    Publicado 2020
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  17. 17
    Clonally heritable gene expression imparts a layer of diversity within cell types

    Clonally heritable gene expression imparts a layer of diversity within cell types por Jeff E. Mold, Martin H. Weissman, Michael Ratz, Michael Hagemann-Jensen, Joanna Hård, Carl‐Johan Eriksson, Hosein Toosi, Joseph Berghenstråhle, Christoph Ziegenhain, Leonie von Berlin, Marcel Martin, Kim Blom, Jens Lagergren, Joakim Lundeberg, Rickard Sandberg, Jakob Michaëlsson, Jonas Frisén

    Publicado 2024
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  18. 18
    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 por 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

    Publicado 2013
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  19. 19
    SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population

    SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population por Adam Ameur, Johan Dahlberg, Pall I. Olason, Francesco Vezzi, Robert Karlsson, Marcel Martin, Johan Viklund, Andreas Kähäri, Pär Lundin, Huiwen Che, Jessada Thutkawkorapin, Jesper Eisfeldt, Samuel Lampa, Mats Dahlberg, Jonas Hagberg, Niclas Jareborg, Ulrika Liljedahl, Inger Jonasson, Åsa Johansson, Lars Feuk, Joakim Lundeberg, Ann‐Christine Syvänen, Sverker Lundin, Daniel Nilsson, Björn Nystedt, Patrik K. E. Magnusson, Ulf Gyllensten

    Publicado 2017
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  20. 20
    From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability

    From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intell... por Anna Lindstrand, Jesper Eisfeldt, Maria Pettersson, Claudia M.B. Carvalho, Malin Kvarnung, Giedre Grigelioniené, Britt‐Marie Anderlid, Olof Bjerin, Peter Gustavsson, Anna Hammarsjö, Patrik Georgii‐Hemming, Erik Iwarsson, Maria Soller, Kristina Lagerstedt‐Robinson, Agne Liedén, Måns Magnusson, Marcel Martin, Helena Malmgren, Magnus Nordenskjöld, Ameli Norling, Ellika Sahlin, Henrik Stranneheim, Emma Tham, Josephine Wincent, Sofia Ygberg, Anna Wedell, Valtteri Wirta, Ann Nordgren, Johanna Lundin, Daniel Nilsson

    Publicado 2019
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