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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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Detalhes bibliográficos
Main Authors: Meacham, Frazer, Boffelli, Dario, Dhahbi, Joseph, Martin, David IK, Singer, Meromit, Pachter, Lior
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2011
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Acesso em linha: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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