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LOCAS – A Low Coverage Assembly Tool for Resequencing Projects
MOTIVATION: Next Generation Sequencing (NGS) is a frequently applied approach to detect sequence variations between highly related genomes. Recent large-scale re-sequencing studies as the Human 1000 Genomes Project utilize NGS data of low coverage to afford sequencing of hundreds of individuals. Her...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2011
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3156226/ https://www.ncbi.nlm.nih.gov/pubmed/21858125 http://dx.doi.org/10.1371/journal.pone.0023455 |