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Sinopsis
Latest generation sequencing revolutionizes the fields of cancer research and oncology. This follow-up volume focuses more extensively on single cell sequencing of cancer and trials in drug resistance. Another exciting feature is the bioinformatics tools given, that can be used on cancer genome studies. Scientists around the world are attempting to find the root cause of cancer. A reasonable cancer treatment plan and potential cure is more optimistic now with the unfolding of the cancer genome. The collective knowledge of how to leverage next generation sequencing in cancer research is paving the way. The important information provided in this volume will move the field forward in developing novel targeted cancer therapies.
"Sinopsis" puede pertenecer a otra edición de este libro.
Acerca del autor
Wei Wu, M.D., Ph.D. is a Research Associate for the Department of Bio Science at the University of Calgary, specializing in the cancer genome and systems biology. He has edited two volumes with Springer. In addition, he's a member of various editorial board for journals including the International Journal of Biomedical Sciences, International Journal of Molecular Medicine and Advances in Sciences and the Research Journal of Biological Sciences. Hani Choudhry, D.Phil is a member of the Genomics Research Group at the Wellcome Trust Centre for Human Genetics at Oxford University. His expertise is in high throughput next generation sequencing.
De la contraportada
Next Generation Sequencing in Cancer Research, Volume 2: From Basepairs to Bedsides, the second in the series Next Generation Sequencing Technology in Cancer Research From Basepairs to Bedsides, is designed to fill the gap between cancer genome research and clinical management of the individual cancer patient. The volume presents the principles of next generation sequencing (NGS) technologies and massively parallel DNA sequencing and their application of the whole genome sequences (WGS), whole exome-seq (WES), RNA-seq, miRNA-seq, and ChIP-seq in cancer research programs and to apply the newly discovered driver genetic alterations for prevention, early diagnosis and genome-oriented precision cancer treatment.
Next Generation Sequencing in Cancer Research, Volume 2: From Basepairs to Bedsides brings together the implementation of a wide range of NGS technologies, including single-cell sequencing, in the clinical setting: discovery and validation of cancer biomarkers; standardization of NGS data production; NGS data reporting systems for clinicians; novel anti-cancer therapies development from NGS data; conducting of clinical trials of newly investigated cancer drugs. It provides compelling evidence to signal a new future for health care and a new standard for cancer care."Sobre este título" puede pertenecer a otra edición de este libro.
- EditorialSpringer-Verlag GmbH
- Año de publicación2016
- ISBN 10 3319376918
- ISBN 13 9783319376912
- EncuadernaciónTapa blanda
- IdiomaInglés
- Número de páginas512
- EditorChoudhry Hani, Wu Wei
- Contacto del fabricanteno disponible
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Next Generation Sequencing in Cancer Research, Volume 2
Publicado por
Springer International Publishing, 2016
ISBN 10: 3319376918
ISBN 13: 9783319376912
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Tapa blanda
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Next Generation Sequencing in Cancer Research, Volume 2
Publicado por
Springer International Publishing Okt 2016, 2016
ISBN 10: 3319376918
ISBN 13: 9783319376912
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Librería: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Alemania
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Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Latest generation sequencing revolutionizes the fields of cancer research and oncology. This follow-up volume focuses more extensively on single cell sequencing of cancer and trials in drug resistance. Another exciting feature is the bioinformatics tools given, that can be used on cancer genome studies. Scientists around the world are attempting to find the root cause of cancer. A reasonable cancer treatment plan and potential cure is more optimistic now with the unfolding of the cancer genome. The collective knowledge of how to leverage next generation sequencing in cancer research is paving the way. The important information provided in this volume will move the field forward in developing novel targeted cancer therapies. 512 pp. Englisch. Nº de ref. del artículo: 9783319376912
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Next Generation Sequencing in Cancer Research, Volume 2 : From Basepairs to Bedsides
Publicado por
Springer International Publishing, 2016
ISBN 10: 3319376918
ISBN 13: 9783319376912
Nuevo
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Librería: AHA-BUCH GmbH, Einbeck, Alemania
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Taschenbuch. Condición: Neu. Druck auf Anfrage Neuware - Printed after ordering - Latest generation sequencing revolutionizes the fields of cancer research and oncology. This follow-up volume focuses more extensively on single cell sequencing of cancer and trials in drug resistance. Another exciting feature is the bioinformatics tools given, that can be used on cancer genome studies. Scientists around the world are attempting to find the root cause of cancer. A reasonable cancer treatment plan and potential cure is more optimistic now with the unfolding of the cancer genome. The collective knowledge of how to leverage next generation sequencing in cancer research is paving the way. The important information provided in this volume will move the field forward in developing novel targeted cancer therapies. Nº de ref. del artículo: 9783319376912
Cantidad disponible: 1 disponibles
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Next Generation Sequencing in Cancer Research, Volume 2
Publicado por
Springer International Publishing, Springer International Publishing Okt 2016, 2016
ISBN 10: 3319376918
ISBN 13: 9783319376912
Nuevo
Taschenbuch
Librería: buchversandmimpf2000, Emtmannsberg, BAYE, Alemania
Calificación del vendedor: 5 de 5 estrellas
Taschenbuch. Condición: Neu. Neuware -Latest generation sequencing revolutionizes the fields ofcancer research and oncology.This follow-up volume focuses more extensivelyonsingle cell sequencing ofcancer and trials in drug resistance. Anotherexciting featureis thebioinformatics tools given,that can be used oncancer genomestudies.Scientists around the world are attempting to find the root cause of cancer. A reasonablecancer treatment plan and potential cure is more optimistic now with the unfolding of the cancer genome. Thecollective knowledge of howto leverage next generation sequencing in cancer research is paving the way.The important information provided in this volumewillmove thefield forward indeveloping noveltargeted cancer therapies.Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 512 pp. Englisch. Nº de ref. del artículo: 9783319376912
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Next Generation Sequencing in Cancer Research, Volume 2: From Basepairs to Bedsides
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Next Generation Sequencing in Cancer Research, Volume 2: From Basepairs to Bedsides
Impresión bajo demandaLibrería: Majestic Books, Hounslow, Reino Unido
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Condición: New. Print on Demand pp. 493. Nº de ref. del artículo: 385544026
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Next Generation Sequencing in Cancer Research, Volume 2: From Basepairs to Bedsides
Impresión bajo demandaLibrería: Biblios, Frankfurt am main, HESSE, Alemania
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Condición: New. PRINT ON DEMAND pp. 493. Nº de ref. del artículo: 18378359951
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