Clinical Genomics
by Shashikant Kulkarni, John Pfeifer
488 pages· 2014· ISBN 9780124051737
About
Clinical Genomics provides an overview of the various next-generation sequencing (NGS) technologies that are currently used in clinical diagnostic laboratories. It presents key bioinformatic challenges and the solutions that must be addressed by clinical genomicists and genomic pathologists, such as specific pipelines for identification of the full range of variants that are clinically important. This book is also focused on the challenges of diagnostic interpretation of NGS results in a clinical setting. Its final sections are devoted to the emerging regulatory issues that will govern clinical use of NGS, and reimbursement paradigms that will affect the way in which laboratory professionals get paid for the testing. Simplifies complexities of NGS technologies for rapid education of clinical genomicists and genomic pathologists towards genomic medicine paradigm Tried and tested practice-based analysis for precision diagnosis and treatment plans Specific pipelines and meta-analysis for full range of clinically important variants
Discuss Clinical Genomics with other readers
Join or start a book club for Clinical Genomics on Readfeed. Live chat, shared reading progress, and AI discussion questions — free to get started.
Frequently asked questions
How do I join a book club for Clinical Genomics?
Sign up free on Readfeed, then browse public clubs or start your own club with Clinical Genomics as the current read. Invite friends with a share link and discuss together with live chat and AI discussion questions.
Can I discuss Clinical Genomics with other readers online?
Yes. Readfeed book clubs let you chat live, share progress, and join discussions about Clinical Genomics with readers worldwide — whether your club is virtual, in-person, or hybrid.
Is Readfeed free?
Yes. Creating an account and joining book clubs is free. Sign up to find readers who love the same books and start discussing today.