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nbCNV: a multi-constrained optimization model for discovering copy number variants in single-cell sequencing data
BACKGROUND: Variations in DNA copy number have an important contribution to the development of several diseases, including autism, schizophrenia and cancer. Single-cell sequencing technology allows the dissection of genomic heterogeneity at the single-cell level, thereby providing important evolutio...
Autores principales: | Zhang, Changsheng, Cai, Hongmin, Huang, Jingying, Song, Yan |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027123/ https://www.ncbi.nlm.nih.gov/pubmed/27639558 http://dx.doi.org/10.1186/s12859-016-1239-7 |
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