Free Delivery Over $100
|
|
|||
|
||||
OverviewCancer Genomics for the Clinician is a practical guide to cancer genomics and its application to cancer diagnosis and care. The book begins with a brief overview of the various types of genetic alterations that are encountered in cancer, followed by accessible and applicable information on next generation sequencing technology and bioinformatics; tumor heterogeneity; whole genome, exome, and transcriptome sequencing; epigenomics; and data analysis and interpretation. Each chapter provides essential explanations of concepts, terminology, and methods. Also included are tips for interpreting and analyzing molecular data, as well as a discussion of molecular predictors for targeted therapies covering hematologic malignancies and solid tumors. The final chapter explains the use of FDA-approved genomic-based targeted therapies for breast cancer, lung cancer, sarcomas, gastrointestinal cancers, urologic cancers, head and neck cancer, thyroid cancer, and many more. Assembled in an accessible format specifically designed for the non-expert, this book provides the clinical oncologist, early career practitioner, and trainee with an essential understanding of the molecular and genetic basis of cancer and the clinical aspects that have led to advancements in diagnosis and treatment. With this resource, physicians and trainees will increase their breadth of knowledge and be better equipped to educate patients and families who want to know more about their genetic predispositions to cancer and the targeted therapies that could be considered and prescribed. Key Features: Describes how cancer genomics and next generation sequencing informs cancer screening, risk factors, therapeutic options, and clinical management across cancer types Explains what mutations are, what tests are needed, and how to interpret the results Provides information on FDA-approved targeted therapies that are being used in the clinic Covers different sequencing platforms and technologies and how they perform in research settings Includes access to the fully searchable eBook Full Product DetailsAuthor: Ramaswamy Govindan , Siddhartha Devarakonda, MDPublisher: Springer Publishing Co Inc Imprint: Springer Publishing Co Inc Dimensions: Width: 12.70cm , Height: 1.30cm , Length: 20.30cm Weight: 0.113kg ISBN: 9780826168672ISBN 10: 0826168671 Pages: 184 Publication Date: 16 January 2019 Audience: Professional and scholarly , Professional & Vocational Format: Paperback Publisher's Status: Active Availability: In stock  We have confirmation that this item is in stock with the supplier. It will be ordered in for you and dispatched immediately. Table of ContentsContents Contributors Preface Acknowledgments 1. Genetic Alterations in Cancer Deepali Jain, Brett H. Herzog, and Leonard B. Maggi, Jr. 2. Tumor Mutational Profiling by Next-Generation Sequencing Samantha N. McNulty, Latisha Love-Gregory, and Jonathan W. Heusel 3. Bioinformatics: What a Clinician Should Know Irena Lanc and Arpad Danos 4. Tumor Heterogeneity Alex H. Wagner, Kilannin Krysiak, Katie M. Campbell, and Erica K. Barnell 5. Epigenetic Alterations in Cancer Erica C. Pehrsson, Hyo Sik Jang, and Ting Wang 6. Cell-Free DNA in Cancer Diagnosis and Follow Up Bruna Pellini Ferreira and Daniel Morgensztern 7. Optimizing Targeted Therapies Using Next-Generation Sequencing Brett H. Herzog and Saiama N. Waqar IndexReviewsAuthor InformationRamaswamy Govindan, MD, Professor of Medicine, Co-Director of Medical Oncology, Washington University School of Medicine, St. Louis, MO Tab Content 6Author Website:Countries AvailableAll regions |
||||
