A carregar...
A Family-Based Rare Haplotype Association Method for Quantitative Traits
BACKGROUND: The variants identified in genome wide association studies account for only a small fraction of disease heritability. A key to this “missing heritability” is believed to be rare variants. Specifically, we focus on rare haplotype variant (rHTV). The existing methods for detecting rHTV are...
Na minha lista:
| Publicado no: | Hum Hered |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6521833/ https://ncbi.nlm.nih.gov/pubmed/30799419 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000493543 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|