Clinical applications for next-generation sequencing / edited by Urszula Demkow, Rafal Ploski.
Material type:
TextPublisher: Amsterdam : Academic Press, 2015Description: 1 volume : illustrations (colour)Content type: text | still image Media type: computer Carrier type: online resourceISBN: 9780128018415 (ebook)Subject(s): Nucleotide sequence | Science | Biology, life sciences | Medical genetics | Medical laboratory testing & techniques | Examination of patients | Molecular biology | Genetics (non-medical) | BiochemistryGenre/Form: Online access: Click here to access online Also available in printed form ISBN 9780128017395Summary: 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.
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Formerly CIP. Uk
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.
Also available in printed form ISBN 9780128017395
Electronic reproduction. Askews and Holts. Mode of access: World Wide Web.
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