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Genome-wide joint analysis of single-nucleotide variant sets and gene expression for hypertension and related phenotypes
BACKGROUND: With the advance of next-generation sequencing technologies, the study of rare variants in targeted genome regions or even the whole genome becomes feasible. Nevertheless, the massive amount of sequencing data brings great computational and statistical challenges for association analyses...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2016
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133505/ https://www.ncbi.nlm.nih.gov/pubmed/27980623 http://dx.doi.org/10.1186/s12919-016-0017-x |