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GapFiller: a de novo assembly approach to fill the gap within paired reads
BACKGROUND: Next Generation Sequencing technologies are able to provide high genome coverages at a relatively low cost. However, due to limited reads' length (from 30 bp up to 200 bp), specific bioinformatics problems have become even more difficult to solve. De novo assembly with short reads,...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439727/ https://www.ncbi.nlm.nih.gov/pubmed/23095524 http://dx.doi.org/10.1186/1471-2105-13-S14-S8 |