Cargando…
Improving variant calling by incorporating known genetic variants into read alignment
Autores principales: | Vo, Nam S, Phan, Vinhthuy |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625095/ http://dx.doi.org/10.1186/1471-2105-16-S15-P18 |
Ejemplares similares
-
A linear model for predicting performance of short-read aligners using genome complexity
por: Tran, Quang, et al.
Publicado: (2015) -
Alignment of short reads to multiple genomes using hashing
por: Tran, Quang, et al.
Publicado: (2014) -
An integrated approach for SNP calling based on population of genomes
por: Vo, Nam S, et al.
Publicado: (2014) -
Fast read alignment with incorporation of known genomic variants
por: Guo, Hongzhe, et al.
Publicado: (2019) -
Exploiting the bootstrap method to analyze patterns of gene expression
por: Vo, Nam S, et al.
Publicado: (2014)