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Comparing a few SNP calling algorithms using low-coverage sequencing data
BACKGROUND: Many Single Nucleotide Polymorphism (SNP) calling programs have been developed to identify Single Nucleotide Variations (SNVs) in next-generation sequencing (NGS) data. However, low sequencing coverage presents challenges to accurate SNV identification, especially in single-sample data....
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2013
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848615/ https://www.ncbi.nlm.nih.gov/pubmed/24044377 http://dx.doi.org/10.1186/1471-2105-14-274 |