Buch, Englisch, 364 Seiten, Format (B × H): 160 mm x 241 mm, Gewicht: 7541 g
ISBN: 978-3-319-56416-6
Verlag: Springer
Will cover the diagnostic yields of various Next Generation Sequencing applications
Readers will learn the advantages and disadvantages of panels and whole exome sequencing as it relates to human genetic disease
Includes a look at future medically relevant exomes
Zielgruppe
Research
Autoren/Hrsg.
Fachgebiete
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Vorklinische Medizin: Grundlagenfächer Humangenetik
- Naturwissenschaften Biowissenschaften Mikrobiologie
- Naturwissenschaften Biowissenschaften Angewandte Biologie Biomathematik
- Naturwissenschaften Biowissenschaften Biowissenschaften Genetik und Genomik (nichtmedizinisch)
Weitere Infos & Material
Part I: overview.- 1. NGS, The new gold standard of identification of defective genes.- 2. Principles of target gene enrichments, pros and cons.- 3. Criteria for clinical application: Full validation and performance characteristics.- 4. Clinical requirements: variant interpretation, confirmation, and turnaround time.- Part II: Experiences in various applications.- 5. The metabolic pathways: GSD, CDG, cobalamin metabolism, and others.- 6. The eye gene panels.- 7. The otogenes.- 8. The immunodeficiency disorders.- 9. The bone density and skeletal related disorders.- 10.The hereditary cancer genes.- 11.The molecular diagnosis of cancers and implications in treatment: Marilyn Li.- 12. Neuromuscular disorders.- 13. The cardiac panel: YuXin Fan, GeneDx or Harvard Partner.- 14. The mitochondrial genome.- 15. The Nuclear Mitomes