Chargement en cours...
Haplotype Kernel Association Test as a Powerful Method to Identify Chromosomal Regions Harboring Uncommon Causal Variants
For most complex diseases, the fraction of heritability that can be explained by the variants discovered from genome-wide association studies is minor. Although the so-called ‘rare variants’ (minor allele frequency [MAF] < 1%) have attracted increasing attention, they are unlikely to account for...
Enregistré dans:
| Auteurs principaux: | , , , , , , , |
|---|---|
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2013
|
| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4116485/ https://ncbi.nlm.nih.gov/pubmed/23740760 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.21740 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|