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...

Descripción completa

Detalles Bibliográficos
Autores principales: Meacham, Frazer, Boffelli, Dario, Dhahbi, Joseph, Martin, David IK, Singer, Meromit, Pachter, Lior
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295828/
https://www.ncbi.nlm.nih.gov/pubmed/22099972
http://dx.doi.org/10.1186/1471-2105-12-451

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295828/
https://www.ncbi.nlm.nih.gov/pubmed/22099972
http://dx.doi.org/10.1186/1471-2105-12-451

Ejemplares similares