Cargando...
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,...
Guardado en:
| Autores principales: | , , |
|---|---|
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BioMed Central
2012
|
| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3439727/ https://ncbi.nlm.nih.gov/pubmed/23095524 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-13-S14-S8 |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|