Abstract
This chapter will explain in brief the principles of genetics and genetic variation and how these apply to prediction of adverse drug reactions and treatment efficacy in cancer. The difference between germline (inherited) and somatic (acquired) genetic variation will be explained and its particular importance in cancer. Some of the different technologies that can now be used to detect genetic variation will be explained. This chapter will also examine how pharmacogenetic studies have been conducted and issues relating to study design comparing different approaches.
Original language | English |
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Title of host publication | Pharmacogenetics |
Subtitle of host publication | Making cancer treatment safer and more effective |
Editors | William G. Newman |
Place of Publication | Dordrecht |
Publisher | Springer Nature |
Chapter | 3 |
Pages | 27-44 |
Number of pages | 18 |
ISBN (Electronic) | 9789048186181 |
ISBN (Print) | 9789048186174 |
DOIs | |
Publication status | Published - 3 Jun 2010 |
Keywords
- genetics
- germline variation
- single nucleotide polymorphism (SNP)
- somatic variation
- pharmacogenetics