Improving de novo sequence assembly using machine learning and comparative genomics for overlap correction

BACKGROUND: With the rapid expansion of DNA sequencing databases, it is now feasible to identify relevant information from prior sequencing projects and completed genomes and apply it to de novo sequencing of new organisms. As an example, this paper demonstrates how such extra information can be use...

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Detalles Bibliográficos
Autores principales: Palmer, Lance E, Dejori, Mathaeus, Bolanos, Randall, Fasulo, Daniel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2824677/
https://www.ncbi.nlm.nih.gov/pubmed/20078885
http://dx.doi.org/10.1186/1471-2105-11-33

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2824677/
https://www.ncbi.nlm.nih.gov/pubmed/20078885
http://dx.doi.org/10.1186/1471-2105-11-33

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