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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...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3156226/ https://ncbi.nlm.nih.gov/pubmed/21858125 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0023455 |
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