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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.
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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.
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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.„Über diesen Titel“ kann sich auf eine andere Ausgabe dieses Titels beziehen.
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Next Generation Sequencing in Cancer Research, Volume 2
Verlag:
Springer International Publishing, 2016
ISBN 10: 3319376918
ISBN 13: 9783319376912
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Next Generation Sequencing in Cancer Research, Volume 2
ISBN 10: 3319376918
ISBN 13: 9783319376912
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Taschenbuch. Zustand: 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. Artikel-Nr. 9783319376912
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Next Generation Sequencing in Cancer Research, Volume 2 : From Basepairs to Bedsides
Verlag:
Springer International Publishing, 2016
ISBN 10: 3319376918
ISBN 13: 9783319376912
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Taschenbuch
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
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Taschenbuch. Zustand: 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. Artikel-Nr. 9783319376912
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