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Clinical Genomics Kulkarni Roy Hardback Academic Press 9780124047488

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Clinical Genomics

Reviews high throughput translational genomic sequencing for diagnosis, prognosis and precision management of inherited and somatic disorders

Shashikant Kulkarni (Edited by), Somak Roy (Edited by)

9780124047488

Hardback, published 12 November 2014

488 pages

27.6 x 21.6 x 2.9 cm, 1.59 kg

\""...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.\"" --Anticancer Research, February 2015

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 i]

Clinical Genomics Kulkarni Roy Hardback Academic Press 9780124047488

Clinical Genomics

Reviews high throughput translational genomic sequencing for diagnosis, prognosis and precision management of inherited and somatic disorders

Shashikant Kulkarni (Edited by), Somak Roy (Edited by)

9780124047488

Hardback, published 12 November 2014

488 pages

27.6 x 21.6 x 2.9 cm, 1.59 kg

\""...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.\"" --Anticancer Research, February 2015

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 i]

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