A carregar...
An analytical workflow for accurate variant discovery in highly divergent regions
BACKGROUND: Current variant discovery methods often start with the mapping of short reads to a reference genome; yet, their performance deteriorates in genomic regions where the reads are highly divergent from the reference sequence. This is particularly problematic for the human leukocyte antigen (...
Na minha lista:
| Publicado no: | BMC Genomics |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5010666/ https://ncbi.nlm.nih.gov/pubmed/27590916 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-016-3045-z |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|