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Clinical Applications for Next-Generation Sequencing
Details
*Clinical Applications for Next Generation Sequencing* provides readers with an outstanding postgraduate resource to learn about the translational use of NGS in clinical environments.
Rooted in both medical genetics and clinical medicine, the book fills the gap between state-of-the-art technology and evidence-based practice, providing an educational opportunity for users to advance patient care by transferring NGS to the needs of real-world patients.
The book builds an interface between genetic laboratory staff and clinical health workers to not only improve communication, but also strengthen cooperation. Users will find valuable tactics they can use to build a systematic framework for understanding the role of NGS testing in both common and rare diseases and conditions, from prenatal care, like chromosomal abnormalities, up to advanced age problems like dementia.
Klappentext
Clinical Applications for Next Generation Sequencing provides readers with an outstanding postgraduate resource to learn about the translational use of NGS in clinical environments.
Rooted in both medical genetics and clinical medicine, the book fills the gap between state-of-the-art technology and evidence-based practice, providing an educational opportunity for users to advance patient care by transferring NGS to the needs of real-world patients.
The book builds an interface between genetic laboratory staff and clinical health workers to not only improve communication, but also strengthen cooperation. Users will find valuable tactics they can use to build a systematic framework for understanding the role of NGS testing in both common and rare diseases and conditions, from prenatal care, like chromosomal abnormalities, up to advanced age problems like dementia.
Inhalt
- Next Generation Sequencing
- Basic Bio-Informatic Analysis of NGS Data
- Analysis of Structural Chromosome Variants by NGS
- NGS in Oncology
- NGS in Hematology
- NGS in Psychiatry and Neurology
- NGS in Dysmorphology
- NGS in Sight and Hearing Impairment
- NGS as a Tool for Non-Invasive Prenatal Diagnostics
- NGS in Cardiology
- NGS - Pharmacogenomics, Individualized Treatment Protocols and Personalized Approach to the Patient
- The Role of NGS in Genetic Counseling
- NGS in Undiagnosed Genetically Based Diseases
- NGS - Organizational and Financial Challenges
- NGS Toward the Future in Clinical Medicine
- Ethical and psychosocial issues in Whole Genome Sequencing (WGS) for newborns
- Next generation sequencing- ethical and social issues (ELSI)
Weitere Informationen
- Allgemeine Informationen
- GTIN 09780128017395
- Genre Biology
- Editor Demkow Urszula, Ploski Rafal
- Sprache Englisch
- Anzahl Seiten 334
- Herausgeber Elsevier Science Publishing Co Inc
- Größe H235mm x B191mm x T20mm
- Jahr 2015
- EAN 9780128017395
- Format Kartonierter Einband
- ISBN 978-0-12-801739-5
- Veröffentlichung 05.10.2015
- Titel Clinical Applications for Next-Generation Sequencing
- Gewicht 680g