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PennCNV in whole-genome sequencing data

BACKGROUND: The use of high-throughput sequencing data has improved the results of genomic analysis due to the resolution of mapping algorithms. Although several tools for copy-number variation calling in whole genome sequencing have been published, the noisy nature of sequencing data is still a lim...

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Detalles Bibliográficos
Autores principales: de Araújo Lima, Leandro, Wang, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629549/
https://www.ncbi.nlm.nih.gov/pubmed/28984186
http://dx.doi.org/10.1186/s12859-017-1802-x