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| Content Provider | Springer Nature Link |
|---|---|
| Author | Pan, Wei |
| Copyright Year | 2008 |
| Abstract | For genome-wide association studies, it has been increasingly recognized that the popular locus-by-locus search for DNA variants associated with disease susceptibility may not be effective, especially when there are interactions between or among multiple loci, for which a multi-loci search strategy may be more productive. However, even if computationally feasible, a genome-wide search over all possible multiple loci requires exploring a huge model space and making costly adjustment for multiple testing, leading to reduced statistical power. On the other hand, there are accumulating data suggesting that protein products of many disease-causing genes tend to interact with each other, or cluster in the same biological pathway. To incorporate this prior knowledge and existing data on gene networks, we propose a gene network-based method to improve statistical power over that of the exhaustive search by giving higher weights to models involving genes nearby in a network. We use simulated data under realistic scenarios, including a large-scale human protein–protein interaction network and 23 known ataxia-causing genes, to demonstrate potential gain by our proposed method when disease-genes are clustered in a network. |
| Starting Page | 225 |
| Ending Page | 234 |
| Page Count | 10 |
| File Format | |
| ISSN | 03406717 |
| Journal | Human Genetics |
| Volume Number | 124 |
| Issue Number | 3 |
| e-ISSN | 14321203 |
| Language | English |
| Publisher | Springer-Verlag |
| Publisher Date | 2008-08-22 |
| Publisher Place | Berlin, Heidelberg |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Metabolic Diseases Gene Function Molecular Medicine Human Genetics |
| Content Type | Text |
| Resource Type | Article |
| Subject | Genetics Genetics (clinical) |
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