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PSE-HMM: Genome-wide CNV detection from NGS data using an HMM with Position-Specific Emission probabilities

Copy Number Variation (CNV) is envisaged to be a major source of large structural variations in the human genome. In recent years, many studies apply Next Generation Sequencing (NGS) data for the CNV detection. However, still there is a necessity to invent more accurate computational tools. |