Sensing the Change
From Molecular Genetics to Personalized Medicine
Seiten
2009
Nova Science Publishers Inc (Verlag)
978-1-60692-217-0 (ISBN)
Nova Science Publishers Inc (Verlag)
978-1-60692-217-0 (ISBN)
How can the giant amount of data obtained in the Human Genome Project and related research endeavours can be used for practical medicine? What are the current problems with phenotype-genotype association studies? This work attempts to further our understanding of biological function from molecular level upwards and to find some of the answers.
How can the giant amount of data obtained in the Human Genome Project and related research endeavours can be used for practical medicine? What are the current problems with phenotype-genotype association studies? How association studies can be applied to the needs of medicinal diagnosis in the framework of personalised medicine? These and many other questions are asked all the time by tens of thousands of researchers from biomedical communities from all over the globe. In this volume, the author attempts to further our understanding of biological function from molecular level upwards and to find some of the answers.
How can the giant amount of data obtained in the Human Genome Project and related research endeavours can be used for practical medicine? What are the current problems with phenotype-genotype association studies? How association studies can be applied to the needs of medicinal diagnosis in the framework of personalised medicine? These and many other questions are asked all the time by tens of thousands of researchers from biomedical communities from all over the globe. In this volume, the author attempts to further our understanding of biological function from molecular level upwards and to find some of the answers.
Introduction; Foreword; The levels of the structural organisation of the human genome; In the wake of classical genetics: the research scenarios in human molecular genetics; Population genetics and implications for the association studies; The genetic association studies; Genetic polymorphisms and personalised medicine; Practical applications of medSNP: the database, the OS and the expert system; Index.
| Zusatzinfo | Illustrations, unspecified |
|---|---|
| Verlagsort | New York |
| Sprache | englisch |
| Maße | 260 x 180 mm |
| Gewicht | 1014 g |
| Themenwelt | Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik |
| ISBN-10 | 1-60692-217-3 / 1606922173 |
| ISBN-13 | 978-1-60692-217-0 / 9781606922170 |
| Zustand | Neuware |
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