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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...
में बचाया:
| मुख्य लेखकों: | , , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
BioMed Central
2010
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2897800/ https://ncbi.nlm.nih.gov/pubmed/20507604 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-0500-3-147 |
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