ABRA: improved coding indel detection via assembly-based realignment

Motivation: Variant detection from next-generation sequencing (NGS) data is an increasingly vital aspect of disease diagnosis, treatment and research. Commonly used NGS-variant analysis tools generally rely on accurately mapped short reads to identify somatic variants and germ-line genotypes. Existi...

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Detalles Bibliográficos
Autores principales: Mose, Lisle E., Wilkerson, Matthew D., Hayes, D. Neil, Perou, Charles M., Parker, Joel S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Applications Notes
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173014/
https://www.ncbi.nlm.nih.gov/pubmed/24907369
http://dx.doi.org/10.1093/bioinformatics/btu376

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173014/
https://www.ncbi.nlm.nih.gov/pubmed/24907369
http://dx.doi.org/10.1093/bioinformatics/btu376

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