A carregar...
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...
Na minha lista:
| Publicado no: | PeerJ |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
PeerJ Inc.
2016
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4918222/ https://ncbi.nlm.nih.gov/pubmed/27350900 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7717/peerj.2139 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|