Wordt geladen...
Testing for rare variant associations in complex diseases
The study of rare variants holds the promise of accounting for some of the missing heritability in complex traits. Next-generation sequencing technologies enable probing of variation across the full spectrum of allele frequencies. Multiple methods for the analysis of rare variants have been proposed...
Bewaard in:
| Hoofdauteurs: | , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2011
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3129640/ https://ncbi.nlm.nih.gov/pubmed/21542888 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm238 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|