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Identification and correction of systematic error in high-throughput sequence data
BACKGROUND: A feature common to all DNA sequencing technologies is the presence of base-call errors in the sequenced reads. The implications of such errors are application specific, ranging from minor informatics nuisances to major problems affecting biological inferences. Recently developed "n...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3295828/ https://ncbi.nlm.nih.gov/pubmed/22099972 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-12-451 |
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