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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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| Publicado no: | BMC Bioinformatics |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4339746/ https://ncbi.nlm.nih.gov/pubmed/25879703 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-015-0483-6 |
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