A carregar...
A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data
BACKGROUND: Rare variants have gathered increasing attention as a possible alternative source of missing heritability. Since next generation sequencing technology is not yet cost-effective for large-scale genomic studies, a widely used alternative approach is imputation. However, the imputation appr...
Na minha lista:
| Publicado no: | BMC Genomics |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4696174/ https://ncbi.nlm.nih.gov/pubmed/26715385 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-015-2192-y |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|