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The Human Genome in Health and Disease
SPAR
kr 177
The Human Genome in Health and Disease

The human genome is a linear sequence of roughly 3 billion bases and information regarding this genome is accumulating at an astonishing rate. Inspired by these advances, The Human Genome in Health and Disease: A Story of Four Letters explores the intimate link between sequence information and biological function. A range of sequence-based functional units of the genome are discussed and illustrated with inherited disorders and cancer. In addition, the book considers valuable medical applications related to human genome sequencing, such as gene therapy methods and the identification of causative mutations in rare genetic disorders.

The primary audiences of the book are students of genetics, biology, medicine, molecular biology and bioinformatics. Richly illustrated with review questions provided for each chapter, the book helps students without previous studies of genetics and molecular biology. It may also be of benefit for advanced non-academics, which in the era of personal genomics, want to learn more about their genome.

 

Key selling features:

  • Molecular sequence perspective, explaining the relationship between DNA sequence motifs and biological function
  • Aids in understanding the functional impact of mutations and genetic variants
  • Material presented at basic level, making it accessible to students without previous studies of genetics and molecular biology
  • Richly illustrated with questions provided to each chapter
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The human genome is a linear sequence of roughly 3 billion bases and information regarding this genome is accumulating at an astonishing rate. Inspired by these advances, The Human Genome in Health and Disease: A Story of Four Letters explores the intimate link between sequence information and biological function. A range of sequence-based functional units of the genome are discussed and illustrated with inherited disorders and cancer. In addition, the book considers valuable medical applications related to human genome sequencing, such as gene therapy methods and the identification of causative mutations in rare genetic disorders.

The primary audiences of the book are students of genetics, biology, medicine, molecular biology and bioinformatics. Richly illustrated with review questions provided for each chapter, the book helps students without previous studies of genetics and molecular biology. It may also be of benefit for advanced non-academics, which in the era of personal genomics, want to learn more about their genome.

 

Key selling features:

  • Molecular sequence perspective, explaining the relationship between DNA sequence motifs and biological function
  • Aids in understanding the functional impact of mutations and genetic variants
  • Material presented at basic level, making it accessible to students without previous studies of genetics and molecular biology
  • Richly illustrated with questions provided to each chapter
Produktdetaljer
Sprog: Engelsk
Sider: 283
ISBN-13: 9780815345916
Indbinding: Paperback
Udgave:
ISBN-10: 0815345917
Kategori: Medicinsk genetik
Udg. Dato: 4 feb 2019
Længde: 13mm
Bredde: 275mm
Højde: 213mm
Oplagsdato: 4 feb 2019
Forfatter(e) Tore (University of Gothenburg Samuelsson, Tore Samuelsson


Kategori Medicinsk genetik


Sprog Engelsk


Indbinding Paperback


Sider 283


Udgave


Længde 13mm


Bredde 275mm


Højde 213mm

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