CNV-seq
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Software:29821
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Related Items (9)
MGP-HMM: detecting genome-wide CNVs using an HMM for modeling mate pair insertion sizes and read counts ⋮ Modeling the next generation sequencing read count data for DNA copy number variant study ⋮ Modeling the evolution space of breakage fusion bridge cycles with a stochastic folding process ⋮ Change-point model on nonhomogeneous Poisson processes with application in copy number profiling by next-generation DNA sequencing ⋮ Modeling read counts for CNV detection in exome sequencing data ⋮ Beta approximation of ratio distribution and its application to next generation sequencing read counts ⋮ An online copy number variant detection method for short sequencing reads ⋮ A Statistical Change-Point Analysis Approach for Modeling the Ratio of Next Generation Sequencing Reads ⋮ A penalized regression approach for DNA copy number study using the sequencing data
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