Vi bøger
Levering: 1 - 2 hverdage

Clinical DNA Variant Interpretation - Bog

- Theory and Practice

Bag om Clinical DNA Variant Interpretation

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. Compiles best practices, methods and sound evidence for DNA variant classification in one applied volumeFeatures chapter contributions from international leaders in the fieldIncludes practical examples of variant classification for common and rare disorders, and across clinical phenotypes

Vis mere
  • Sprog:
  • Engelsk
  • ISBN:
  • 9780128205198
  • Indbinding:
  • Paperback
  • Sideantal:
  • 436
  • Udgivet:
  • 2. marts 2021
  • Størrelse:
  • 236x193x27 mm.
  • Vægt:
  • 880 g.
  • Ukendt - mangler pt..

Normalpris

Medlemspris

Prøv i 30 dage for 45 kr.
Herefter fra 79 kr./md. Ingen binding.

Beskrivelse af Clinical DNA Variant Interpretation

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.

Compiles best practices, methods and sound evidence for DNA variant classification in one applied volumeFeatures chapter contributions from international leaders in the fieldIncludes practical examples of variant classification for common and rare disorders, and across clinical phenotypes

Brugerbedømmelser af Clinical DNA Variant Interpretation



Gør som tusindvis af andre bogelskere

Tilmeld dig nyhedsbrevet og få gode tilbud og inspiration til din næste læsning.