CNV-seq

swMATH17970MaRDI QIDQ29821FDOQ29821

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Cited In (9)

• An online copy number variant detection method for short sequencing reads
• MGP-HMM: detecting genome-wide CNVs using an HMM for modeling mate pair insertion sizes and read counts
• 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
• A penalized regression approach for DNA copy number study using the sequencing data
• Modeling the next generation sequencing read count data for DNA copy number variant study
• Beta approximation of ratio distribution and its application to next generation sequencing read counts
• Modeling the evolution space of breakage fusion bridge cycles with a stochastic folding process
• A Statistical Change-Point Analysis Approach for Modeling the Ratio of Next Generation Sequencing Reads

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