Loading...
Haplotype-based methods for detecting uncommon causal variants with common SNPs
Detecting uncommon causal variants (minor allele frequency (MAF) < 5%) is difficult with commercial single-nucleotide polymorphism (SNP) arrays that are designed to capture common variants (MAF > 5%). Haplotypes can provide insights into underlying linkage disequilibrium (LD) structure and can...
Na minha lista:
| Main Authors: | , , , , , , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2012
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3513398/ https://ncbi.nlm.nih.gov/pubmed/22706849 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.21650 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|