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Clinical DNA Variant Interpretation

Theory and Practice

Specificaties
Paperback, blz. | Engels
Elsevier Science | e druk, 2021
ISBN13: 9780128205198
Rubricering
Elsevier Science e druk, 2021 9780128205198
€ 187,00
Levertijd ongeveer 8 werkdagen

Samenvatting

Clinical DNA Variant Interpretation: Theory and Practice, a new volume in the Translational and Applied Genomics series, covers foundational aspects, modes of analysis, technology, disease and disorder specific case studies, and clinical integration. This book provides a deep theoretical background, as well as applied case studies and methodology, enabling researchers, clinicians and healthcare providers to effectively classify DNA variants associated with disease and patient phenotypes. Practical chapters discuss genomic variant interpretation, terminology and nomenclature, international consensus guidelines, population allele frequency, functional evidence transcripts for RNA, proteins, and enzymes, somatic mutations, somatic profiling, and much more.

Specificaties

ISBN13:9780128205198
Taal:Engels
Bindwijze:Paperback

Inhoudsopgave

<p>1. Introduction: The challenge of genomic DNA interpretation </p> <p>Section I. Theoretical Chapters<br>2. General considerations: Terminology and standards<br>3. International consensus guidelines for constitutional sequence variant interpretation<br>4. Quantitative modelling: Multifactorial integration of data <br>5. Clinical and genetic evidence and population evidence<br>6. The computational approach to variant interpretation: principles, results, and applicability<br>7. Functional evidence (I) transcripts and RNA splicing outline<br>8. Functional evidence (II) protein and enzyme function <br>9. Somatic data usage for classification of germline variants <br>10. Pharmacogenomics and personalized medicine<br>11. Data sharing and gene variant databases<br>12. Approaches to the comprehensive interpretation of genome-scale sequencing<br>13. Phenotype evaluation and clinical context: Application of case-level data in genomic variant interpretation </p> <p>Section II. Practical Chapters<br>14. Inherited cardiomyopathies<br>15. Phenylketonuria<br>16. Hearing loss<br>17. Familial hypercholesterolemia<br>18. Classification of genetic variants in hereditary cancer genes<br>19. RASopathies <br>20. Summary and conclusions</p>
€ 187,00
Levertijd ongeveer 8 werkdagen

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        Clinical DNA Variant Interpretation