A machine learning framework for genotyping the structural variations with copy number variant

BACKGROUND: Genotyping of structural variation is an important computational problem in next generation sequence data analysis. However, in cancer genomes, the copy number variant(CNV) often coexists with other types of structural variations which significantly reduces the accuracy of the existing g...

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Detalles Bibliográficos
Autores principales: Zheng, Tian, Zhu, Xiaoyan, Zhang, Xuanping, Zhao, Zhongmeng, Yi, Xin, Wang, Jiayin, Li, Hongle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450592/
https://www.ncbi.nlm.nih.gov/pubmed/32854699
http://dx.doi.org/10.1186/s12920-020-00733-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450592/
https://www.ncbi.nlm.nih.gov/pubmed/32854699
http://dx.doi.org/10.1186/s12920-020-00733-w

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