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Published by Taylor & Francis Ltd, 2025
ISBN 10: 1032392622 ISBN 13: 9781032392622
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Published by Taylor & Francis Ltd, London, 2025
ISBN 10: 1032392622 ISBN 13: 9781032392622
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Hardcover. Condition: new. Hardcover. This cutting-edge reference book compiles standard operating procedures, protocols, and applications of next-generation sequencing (NGS). It discusses genomic testing applications through NGS. It pays special focus on the protocols for cataloguing variants of uncertain significance. Over the years, NGS and advanced bioinformatics approaches have allowed the transition of genomic assays into translational practices. The book covers visualisation of NGS datasets, investigation of early development impairment, and metagenome protocols. It also discusses the challenges in NGS methods.Key Points:Includes case studies of application of NGS in different taxa like humans, rodents, plants, and bacteriaCompiles protocols from various reputed companies like Illumina, PacBio, and ThermoFisherDiscusses the translational applications of NGS methodsReviews machine learning heuristics for NGS data interpretationDiscusses emerging genomic assay technologies and characterising mechanisms of disease prevalenceThe book is meant for researchers and industry experts in genomics, computational biology, and bioinformatics.Chapter 7 and 9 of this book is freely available as a downloadable Open Access PDF at under a Creative Commons [Attribution-Non Commercial-No Derivatives (CC BY-NC-ND)] 4.0 license. This reference book compiles standard operating procedures, protocols, and applications of Next-Generation Sequencing (NGS). It discusses genomic testing applications through NGS and protocols for cataloging variants of uncertain significance. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
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Published by Taylor & Francis Ltd, London, 2025
ISBN 10: 1032392622 ISBN 13: 9781032392622
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Add to basketHardcover. Condition: new. Hardcover. This cutting-edge reference book compiles standard operating procedures, protocols, and applications of next-generation sequencing (NGS). It discusses genomic testing applications through NGS. It pays special focus on the protocols for cataloguing variants of uncertain significance. Over the years, NGS and advanced bioinformatics approaches have allowed the transition of genomic assays into translational practices. The book covers visualisation of NGS datasets, investigation of early development impairment, and metagenome protocols. It also discusses the challenges in NGS methods.Key Points:Includes case studies of application of NGS in different taxa like humans, rodents, plants, and bacteriaCompiles protocols from various reputed companies like Illumina, PacBio, and ThermoFisherDiscusses the translational applications of NGS methodsReviews machine learning heuristics for NGS data interpretationDiscusses emerging genomic assay technologies and characterising mechanisms of disease prevalenceThe book is meant for researchers and industry experts in genomics, computational biology, and bioinformatics.Chapter 7 and 9 of this book is freely available as a downloadable Open Access PDF at under a Creative Commons [Attribution-Non Commercial-No Derivatives (CC BY-NC-ND)] 4.0 license. This reference book compiles standard operating procedures, protocols, and applications of Next-Generation Sequencing (NGS). It discusses genomic testing applications through NGS and protocols for cataloging variants of uncertain significance. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
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Published by Taylor & Francis Ltd, London, 2025
ISBN 10: 1032392622 ISBN 13: 9781032392622
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Hardcover. Condition: new. Hardcover. This cutting-edge reference book compiles standard operating procedures, protocols, and applications of next-generation sequencing (NGS). It discusses genomic testing applications through NGS. It pays special focus on the protocols for cataloguing variants of uncertain significance. Over the years, NGS and advanced bioinformatics approaches have allowed the transition of genomic assays into translational practices. The book covers visualisation of NGS datasets, investigation of early development impairment, and metagenome protocols. It also discusses the challenges in NGS methods.Key Points:Includes case studies of application of NGS in different taxa like humans, rodents, plants, and bacteriaCompiles protocols from various reputed companies like Illumina, PacBio, and ThermoFisherDiscusses the translational applications of NGS methodsReviews machine learning heuristics for NGS data interpretationDiscusses emerging genomic assay technologies and characterising mechanisms of disease prevalenceThe book is meant for researchers and industry experts in genomics, computational biology, and bioinformatics.Chapter 7 and 9 of this book is freely available as a downloadable Open Access PDF at under a Creative Commons [Attribution-Non Commercial-No Derivatives (CC BY-NC-ND)] 4.0 license. This reference book compiles standard operating procedures, protocols, and applications of Next-Generation Sequencing (NGS). It discusses genomic testing applications through NGS and protocols for cataloging variants of uncertain significance. This item is printed on demand. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.
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Buch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - This reference book compiles standard operating procedures, protocols, and applications of Next-Generation Sequencing (NGS). It discusses genomic testing applications through NGS and protocols for cataloging variants of uncertain significance.