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Utilizing mutual information for detecting rare and common variants associated with a categorical trait
Background. Genome-wide association studies have succeeded in detecting novel common variants which associate with complex diseases. As a result of the fast changes in next generation sequencing technology, a large number of sequencing data are generated, which offers great opportunities to identify...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
PeerJ Inc.
2016
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918222/ https://www.ncbi.nlm.nih.gov/pubmed/27350900 http://dx.doi.org/10.7717/peerj.2139 |