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ParMap, an algorithm for the identification of small genomic insertions and deletions in nextgen sequencing data
BACKGROUND: Next-generation sequencing produces high-throughput data, albeit with greater error and shorter reads than traditional Sanger sequencing methods. This complicates the detection of genomic variations, especially, small insertions and deletions. FINDINGS: Here we describe ParMap, a statist...
| Autores principales: | , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2897800/ https://www.ncbi.nlm.nih.gov/pubmed/20507604 http://dx.doi.org/10.1186/1756-0500-3-147 |