Comparative study of tools for copy number variation detection using next-generation sequencing data
Copy number variation (CNV) plays an important role in disease susceptibility as a type of intermediate-scale structural variation (SV). Accurate CNV detection is crucial for understanding human ...
Copy number variation (CNV) is a type of structural variation ranging from 50 to several million base pairs (bp) 1,2,3,4,5. It is an unbalanced variation where a segment of the human genome can be ...
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