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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Detalles Bibliográficos
Autores principales: Klein, Juliane D., Ossowski, Stephan, Schneeberger, Korbinian, Weigel, Detlef, Huson, Daniel H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
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

Internet

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

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