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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...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
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| Materias: | |
| 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 |