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Next Generation Sequencing Technologies in Medical Genetics

Specificaties
Paperback, 94 blz. | Engels
Springer New York | 2013e druk, 2013
ISBN13: 9781461490319
Rubricering
Springer New York 2013e druk, 2013 9781461490319
Onderdeel van serie SpringerBriefs in Genetics
€ 86,39
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Samenvatting

This book introduces readers to Next Generation Sequencing applications in medical genetics. The authors discuss the direct application of next-generation sequencing to medicine, specifically, laboratory medicine or molecular diagnostics. The first part of the book contains chapters on sanger sequencing, NGS technologies, targeted-amplification and capture, and exome sequencing. The second part of the book focuses on genetic disorders diagnoses by NGS, prenatal diagnosis, muscular dystrophies, mitochondrial disorders diagnosis, and challenges in molecular diagnosis. Recent developments and potential future trends in NGS sequencing applications are highlighted, as well.​

Specificaties

ISBN13:9781461490319
Taal:Engels
Bindwijze:paperback
Aantal pagina's:94
Uitgever:Springer New York
Druk:2013

Inhoudsopgave

<p>Sanger sequencing principles, history and landmarks.- A survey of next-generation sequencing technologies.- A review of DNA enrichment technologies.- Application of next-generation sequencing to the diagnosis of genetic disorders a brief overview.- Next-generation sequencing-based noninvasive prenatal diagnosis.- Diagnosis of inherited neuromuscular disorders by next-generation sequencing.- Application of next-generation sequencing in hearing loss diagnosis.- Exome sequencing as a discovery and a diagnostic tool.- Challenges of next-generation sequencing-based molecular diagnostics.</p>
€ 86,39
Levertijd ongeveer 9 werkdagen
Gratis verzonden

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        Next Generation Sequencing Technologies in Medical Genetics