A copy number variation detection method based on OCSVM algorithm using multi strategies integration
Copy number variation (CNV) is an important part of human genetic variations, which is associated with various kinds of diseases. To tackle the limitations of ...
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 ...
However, ES is not the first choice for detecting copy number variants (CNVs), which are typically deletions or duplications of DNA segments. CNVs cause a significant proportion of genetic disorders.
A new analysis explores the genetic liability of psychiatric disorders using polygenic scores and recurrent copy number variants.
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