RNA-Seq provides an ideal platform to study the complete set of transcripts for a specific developmental stage or physiological condition. It reveals not only expression-level changes, but also structural changes in the coding sequences, including gene rearrangements. In this dissertation, I present my contributions to the development of computational tools for the robust and efficient analysis of RNA-Seq data to support cancer research. To automate the laborious and computationally intensive procedure of RNA-Seq data management, I worked on the development of Hydra, an RNA-Seq pipeline for the parallel processing and quality control of large numbers of samples. I then present QueryFuse, a novel gene-specific fusion-detection algorithm for aligned RNA-Seq data. It is designed to help biologists find and/or computationally validate fusions of interest quickly, and to annotate the detected events with visualization and detailed properties of the supporting reads. Finally, I contributed to the identification of a novel fusion event in lymphoma, with potential therapeutic implications in clinical samples. I validated this fusion in silico and by experimental validation.
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
RNA-Seq provides an ideal platform to study the complete set of transcripts for a specific developmental stage or physiological condition. It reveals not only expression-level changes, but also structural changes in the coding sequences, including gene rearrangements. In this dissertation, I present my contributions to the development of computational tools for the robust and efficient analysis of RNA-Seq data to support cancer research. To automate the laborious and computationally intensive procedure of RNA-Seq data management, I worked on the development of Hydra, an RNA-Seq pipeline for the parallel processing and quality control of large numbers of samples. I then present QueryFuse, a novel gene-specific fusion-detection algorithm for aligned RNA-Seq data. It is designed to help biologists find and/or computationally validate fusions of interest quickly, and to annotate the detected events with visualization and detailed properties of the supporting reads. Finally, I contributed to the identification of a novel fusion event in lymphoma, with potential therapeutic implications in clinical samples. I validated this fusion in silico and by experimental validation.
Current:Post-doctoral fellowship, Bio-medical Transnational Research Institute of Jinan University, ChinaPh.D., Bioinformatics, Boston University School of Medicine, Boston,Research interest: Computational applications in cancer research and human microbiome.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -RNA-Seq provides an ideal platform to study the complete set of transcripts for a specific developmental stage or physiological condition. It reveals not only expression-level changes, but also structural changes in the coding sequences, including gene rearrangements. In this dissertation, I present my contributions to the development of computational tools for the robust and efficient analysis of RNA-Seq data to support cancer research. To automate the laborious and computationally intensive procedure of RNA-Seq data management, I worked on the development of Hydra, an RNA-Seq pipeline for the parallel processing and quality control of large numbers of samples. I then present QueryFuse, a novel gene-specific fusion-detection algorithm for aligned RNA-Seq data. It is designed to help biologists find and/or computationally validate fusions of interest quickly, and to annotate the detected events with visualization and detailed properties of the supporting reads. Finally, I contributed to the identification of a novel fusion event in lymphoma, with potential therapeutic implications in clinical samples. I validated this fusion in silico and by experimental validation. 108 pp. Englisch. N° de réf. du vendeur 9783659870873
Quantité disponible : 2 disponible(s)
Vendeur : Books Puddle, New York, NY, Etats-Unis
Etat : New. N° de réf. du vendeur 26404731280
Quantité disponible : 4 disponible(s)
Vendeur : Majestic Books, Hounslow, Royaume-Uni
Etat : New. Print on Demand. N° de réf. du vendeur 409471567
Quantité disponible : 4 disponible(s)
Vendeur : moluna, Greven, Allemagne
Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Tan YuxiangCurrent:Post-doctoral fellowship, Bio-medical Transnational Research Institute of Jinan University, ChinaPh.D., Bioinformatics, Boston University School of Medicine, Boston,Research interest: Computational applications in . N° de réf. du vendeur 159146715
Quantité disponible : Plus de 20 disponibles
Vendeur : Biblios, Frankfurt am main, HESSE, Allemagne
Etat : New. PRINT ON DEMAND. N° de réf. du vendeur 18404731290
Quantité disponible : 4 disponible(s)
Vendeur : Revaluation Books, Exeter, Royaume-Uni
Paperback. Etat : Brand New. 108 pages. 8.66x5.91x0.25 inches. In Stock. N° de réf. du vendeur 3659870870
Quantité disponible : 1 disponible(s)
Vendeur : buchversandmimpf2000, Emtmannsberg, BAYE, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -RNA-Seq provides an ideal platform to study the complete set of transcripts for a specific developmental stage or physiological condition. It reveals not only expression-level changes, but also structural changes in the coding sequences, including gene rearrangements. In this dissertation, I present my contributions to the development of computational tools for the robust and efficient analysis of RNA-Seq data to support cancer research. To automate the laborious and computationally intensive procedure of RNA-Seq data management, I worked on the development of Hydra, an RNA-Seq pipeline for the parallel processing and quality control of large numbers of samples. I then present QueryFuse, a novel gene-specific fusion-detection algorithm for aligned RNA-Seq data. It is designed to help biologists find and/or computationally validate fusions of interest quickly, and to annotate the detected events with visualization and detailed properties of the supporting reads. Finally, I contributed to the identification of a novel fusion event in lymphoma, with potential therapeutic implications in clinical samples. I validated this fusion in silico and by experimental validation.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 108 pp. Englisch. N° de réf. du vendeur 9783659870873
Quantité disponible : 1 disponible(s)
Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - RNA-Seq provides an ideal platform to study the complete set of transcripts for a specific developmental stage or physiological condition. It reveals not only expression-level changes, but also structural changes in the coding sequences, including gene rearrangements. In this dissertation, I present my contributions to the development of computational tools for the robust and efficient analysis of RNA-Seq data to support cancer research. To automate the laborious and computationally intensive procedure of RNA-Seq data management, I worked on the development of Hydra, an RNA-Seq pipeline for the parallel processing and quality control of large numbers of samples. I then present QueryFuse, a novel gene-specific fusion-detection algorithm for aligned RNA-Seq data. It is designed to help biologists find and/or computationally validate fusions of interest quickly, and to annotate the detected events with visualization and detailed properties of the supporting reads. Finally, I contributed to the identification of a novel fusion event in lymphoma, with potential therapeutic implications in clinical samples. I validated this fusion in silico and by experimental validation. N° de réf. du vendeur 9783659870873
Quantité disponible : 1 disponible(s)
Vendeur : preigu, Osnabrück, Allemagne
Taschenbuch. Etat : Neu. Computational Approaches for Transcriptome Cancer Analysis by RNA-Seq | Yuxiang Tan | Taschenbuch | 108 S. | Englisch | 2016 | LAP LAMBERT Academic Publishing | EAN 9783659870873 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu. N° de réf. du vendeur 103670650
Quantité disponible : 5 disponible(s)