Abstract
There has been increasing interest in rare variants and their association with disease, and several rare variantdisease associations have already been detected. The usual association tests for common variants are underpowered for detecting variants of lower frequency, so alternative approaches are required. In addition to reviewing the association analysis methods for rare variants, we discuss the limitations of genome-wide association studies in identifying rare variants and the problems that arise in the imputation of rare variants.
Original language | English |
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Pages (from-to) | 293-308 |
Number of pages | 16 |
Journal | Annual Review of Genetics |
Volume | 44 |
DOIs | |
State | Published - 1 Dec 2010 |
Externally published | Yes |
Keywords
- 1,000 genomes project
- collapsing method
- imputation
- sequencing