TY  - CHAP
AU  - Kok-Siong Poon
AU  - Julian Wei-Tze Tang
AU  - Evelyn Siew- Chuan Koay
ED  - Ali Samadikuchaksaraei
ED  - Morteza Seifi
Y1  - 2019-03-20
PY  - 2019
T1  - HCV Genotyping with Concurrent Profiling of Resistance-Associated Variants by NGS Analysis
N2  - Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for development of many human diseases. This book addresses the methods of detection, analysis, and interpretation of genomic variations in clinically relevant scenarios. If your research or clinical practice involves handling of genomic sequencing data, this book is for you. Topics covered include: methods for identifying genetic diversity, the workflow for analyzing whole exome and whole genome sequencing data, local ancestry deconvolution models, the value of molecular patterns and pattern biomarkers in cancer diagnosis and prognosis, and genotyping and profiling resistance-associated variants of hepatitis C. If your research or clinical practice involves handling of genomic sequencing data, this book is for you.
BT  - Bioinformatics Tools for Detection and Clinical Interpretation of Genomic Variations
SP  - Ch. 5
UR  - https://doi.org/10.5772/intechopen.84577
DO  - 10.5772/intechopen.84577
SN  - 978-1-78923-800-6
PB  - IntechOpen
CY  - Rijeka
Y2  - 2024-05-11
ER  -