Improving de novo sequence assembly using machine learning and comparative genomics for overlap correction
<p>Abstract</p> <p>Background</p> <p>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 <it>de novo </it>sequencing of new organisms. As an example, this paper demonstrates how...
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| Principais autores: | , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BMC
2010-01-01
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| Serier: | BMC Bioinformatics |
| Online adgang: | http://www.biomedcentral.com/1471-2105/11/33 |
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