Carregant...

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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:BMC Bioinformatics
Autors principals: de Araújo Lima, Leandro, Wang, Kai
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2017
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5629549/
https://ncbi.nlm.nih.gov/pubmed/28984186
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1802-x
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!