AluScanCNV2: An R package for copy number variation calling and cancer risk prediction with next-generation sequencing data

The usage of next-generation sequencing (NGS) to detect copy number variation (CNV) is widely accepted in cancer research. Based on an AluScanCNV software developed by us previously, an AluScanCNV2 software has been developed in the present study as an R package that performs CNV detection from NGS...

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Detalles Bibliográficos
Autores principales: Hu, Taobo, Chen, Si, Ullah, Ata, Xue, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411622/
https://www.ncbi.nlm.nih.gov/pubmed/30906832
http://dx.doi.org/10.1016/j.gendis.2018.09.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411622/
https://www.ncbi.nlm.nih.gov/pubmed/30906832
http://dx.doi.org/10.1016/j.gendis.2018.09.001

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