Abstract
Summary: Chromosomal copy number variation (CNV) refers to a polymorphism that a DNA segment presents deletion or duplication in the population. The computational algorithms developed to identify this type of variation are usually of high computational complexity. Here we present a user-friendly R package, modSaRa, designed to perform copy number variants identification. The package is developed based on a change-point based method with optimal computational complexity and desirable accuracy. The current version of modSaRa package is a comprehensive tool with integration of preprocessing steps and main CNV calling steps.
Cite
CITATION STYLE
Xiao, F., Niu, Y., Hao, N., Xu, Y., Jin, Z., & Zhang, H. (2017). ModSaRa: A computationally efficient R package for CNV identification. Bioinformatics, 33(15), 2384–2385. https://doi.org/10.1093/bioinformatics/btx212
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