HAPGEN2
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Software:29214
swMATH17354MaRDI QIDQ29214FDOQ29214
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Cited In (5)
- Title not available (Why is that?)
- A novel SNP-set analytical method without distinguishing common variants or rare variants in genome-wide association study
- Pathway-based kernel boosting for the analysis of genome-wide association studies
- Replicability analysis for genome-wide association studies
- Genetic variant set-based tests using the generalized Berk-Jones statistic with application to a genome-wide association study of breast cancer
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