Identification of indels in next-generation sequencing data

BACKGROUND: The discovery and mapping of genomic variants is an essential step in most analysis done using sequencing reads. There are a number of mature software packages and associated pipelines that can identify single nucleotide polymorphisms (SNPs) with a high degree of concordance. However, th...

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Detalles Bibliográficos
Autores principales: Ratan, Aakrosh, Olson, Thomas L, Loughran, Thomas P, Miller, Webb
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339746/
https://www.ncbi.nlm.nih.gov/pubmed/25879703
http://dx.doi.org/10.1186/s12859-015-0483-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339746/
https://www.ncbi.nlm.nih.gov/pubmed/25879703
http://dx.doi.org/10.1186/s12859-015-0483-6

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