Andere Kunden interessierten sich auch für
![Antioxidant and Redox Regulation of Genes]( "Antioxidant and Redox Regulation of Genes")
Antioxidant and Redox Regulation of Genes125,99 €![Cytochrome P450, Part C]( "Cytochrome P450, Part C")
Cytochrome P450, Part C124,99 €![Advances in DNA Sequence-Specific Agents]( "Advances in DNA Sequence-Specific Agents")
Advances in DNA Sequence-Specific Agents72,99 €![Economic Evaluation in Genomic Medicine]( "Economic Evaluation in Genomic Medicine")
Economic Evaluation in Genomic Medicine48,99 €![Advances in Enzyme Regulation]( "Advances in Enzyme Regulation")
Advances in Enzyme Regulation497,99 €![Chronobiology: Biological Timing in Health and Disease]( "Chronobiology: Biological Timing in Health and Disease")
Chronobiology: Biological Timing in Health and Disease94,99 €![DNA Methylation and Complex Human Disease]( "DNA Methylation and Complex Human Disease")
DNA Methylation and Complex Human Disease81,99 €
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.
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.