يعرض 1 - 6 نتائج من 6 نتيجة بحث عن '"Whole-exome and RNA sequencing"', وقت الاستعلام: 1.02s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Microsatellite instability at U2AF-binding polypyrimidic tract sites perturbs alternative splicing during colorectal cancer initiation

    المؤلفون: Vincent Jonchère, Hugo Montémont, Enora Le Scanf, Aurélie Siret, Quentin Letourneur, Emmanuel Tubacher, Christophe Battail, Assane Fall, Karim Labreche, Victor Renault, Toky Ratovomanana, Olivier Buhard, Ariane Jolly, Philippe Le Rouzic, Cody Feys, Emmanuelle Despras, Habib Zouali, Rémy Nicolle, Pascale Cervera, Magali Svrcek, Pierre Bourgoin, Hélène Blanché, Anne Boland, Jérémie Lefèvre, Yann Parc, Mehdi Touat, Franck Bielle, Danielle Arzur, Gwennina Cueff, Catherine Le Jossic-Corcos, Gaël Quéré, Gwendal Dujardin, Marc Blondel, Cédric Le Maréchal, Romain Cohen, Thierry André, Florence Coulet, Pierre de la Grange, Aurélien de Reyniès, Jean-François Fléjou, Florence Renaud, Agusti Alentorn, Laurent Corcos, Jean-François Deleuze, Ada Collura, Alex Duval

    المصدر: Genome Biology, Vol 25, Iss 1, Pp 1-26 (2024)

    مصطلحات موضوعية: Colorectal cancer, Mismatch repair deficiency, Microsatellite instability, Whole-exome and RNA sequencing, Alternative splicing, Polypyrimidine U2AF binding site, Biology (General), QH301-705.5, Genetics, QH426-470

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/1474-760X

    URL الوصول: https://doaj.org/article/87efc7be65b6480c8bf4509103a6aab4

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  2. 2
    دورية أكاديمية
    Microsatellite instability at U2AF-binding polypyrimidic tract sites perturbs alternative splicing during colorectal cancer initiation

    المؤلفون: Jonchère, Vincent, Montémont, Hugo, Le Scanf, EnoraAff2, Aff3, Siret, Aurélie, Letourneur, Quentin, Tubacher, Emmanuel, Battail, Christophe, Fall, Assane, Labreche, Karim, Renault, Victor, Ratovomanana, Toky, Buhard, Olivier, Jolly, Ariane, Le Rouzic, Philippe, Feys, Cody, Despras, Emmanuelle, Zouali, Habib, Nicolle, Rémy, Cervera, PascaleAff1, Aff8, Svrcek, MagaliAff1, Aff8, Bourgoin, PierreAff1, Aff8, Blanché, Hélène, Boland, Anne, Lefèvre, JérémieAff1, Aff9, Parc, YannAff1, Aff9, Touat, MehdiAff1, Aff10, Bielle, Franck, Arzur, DanielleAff2, Aff3, Cueff, GwenninaAff2, Aff3, Le Jossic-Corcos, CatherineAff2, Aff3, Quéré, GaëlAff2, Aff3, Dujardin, GwendalAff2, Aff3, Blondel, MarcAff2, Aff3, Le Maréchal, CédricAff2, Aff3, Cohen, RomainAff1, Aff12, André, ThierryAff1, Aff12, Coulet, FlorenceAff1, Aff13, de la Grange, Pierre, de Reyniès, Aurélien, Fléjou, Jean-FrançoisAff1, Aff8, Renaud, Florence, Alentorn, Agusti, Corcos, LaurentAff2, Aff3, Deleuze, Jean-FrançoisAff4, Aff5, Collura, Ada, Duval, AlexAff1, Aff13, IDs13059024033405_cor46

    المصدر: Genome Biology. 25(1)

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  3. 3
    دورية أكاديمية
    Main Strategies for the Identification of Neoantigens

    المؤلفون: Alexander V. Gopanenko, Ekaterina N. Kosobokova, Vyacheslav S. Kosorukov

    المصدر: Cancers, Vol 12, Iss 10, p 2879 (2020)

    مصطلحات موضوعية: neoantigens, whole-exome and RNA sequencing, peptide-MHC binding predictions, pMHC-TCR binding predictions, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

    وصف الملف: electronic resource

    Relation: https://www.mdpi.com/2072-6694/12/10/2879; https://doaj.org/toc/2072-6694

    URL الوصول: https://doaj.org/article/cc40e376a474439bb573b93863d986ee

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  4. 4
    دورية أكاديمية

    لا يتم عرض هذه النتيجة على الضيوف.

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  5. 5
    Identification of Novel Point Mutations in Splicing Sites by the Integration of Exome and RNA Sequencing Data in Myeloproliferative Diseases

    المؤلفون: Hima Raman, Roberta Spinelli, Rocco Piazza, Alessandra Stasia, Carlo Gambacorti-Passerini, Alessandra Pirola, Simona Valletta

    المساهمون: Spinelli, R, Piazza, R, Raman, H, Pirola, A, Valletta, S, Stasia, A, GAMBACORTI PASSERINI, C

    المصدر: Blood. 118:2462-2462

    مصطلحات موضوعية: Genetics, Sanger sequencing, Splice site mutation, Somatic mutations, Splicing variants, Whole-Exome sequencing, RNA sequencing, high-throughput sequencing, Immunology, Alternative splicing, Intron, Cell Biology, Hematology, Biology, Biochemistry, Exon, symbols.namesake, MED/15 - MALATTIE DEL SANGUE, RNA splicing, symbols, Exome, Exome sequencing

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f086877c9f215cad081b8a89e145b4f
    https://doi.org/10.1182/blood.v118.21.2462.2462

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  6. 6
    مورد إلكتروني
    Identification of Novel Point Mutations in Splicing Sites by the Integration of Exome and RNA Sequencing Data in Myeloproliferative Diseases

    مصطلحات الفهرس: Somatic mutations, Splicing variants, Whole-Exome sequencing, RNA sequencing, high-throughput sequencing, MED/15 - MALATTIE DEL SANGUE, info:eu-repo/semantics/conferenceObject

    URL: http://hdl.handle.net/10281/37553
    info:eu-repo/semantics/altIdentifier/wos/WOS:000299597103328
    ispartofbook:ASH 2011; 53rd Congress of the American Society of Hematology
    53rd Annual Meeting of the American Society of Hematology
    volume:118
    issue:21
    firstpage:1055
    lastpage:1056
    numberofpages:2
    journal:BLOOD

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