ExonCNV This tool uses a more sensitive copy number variation detection algorithm, and develops a complete set of interactive systems in combination with visualization methods.

Copy number variation is one of the common forms of variation in genomic structural variation, and is closely related to the occurrence and development of many diseases including cancer. With the rapid development of high-throughput sequencing technology, the mainstream of copy number variation detection is based on sequencing data. At present, the copy number variation detection algorithm based on exon sequencing data improves the accuracy of detection while reducing costs. However, due to insufficient consideration of the influence of noise, the sensitivity needs to be further improved.

This tool uses a more sensitive copy number variation detection algorithm, and develops a complete set of interactive systems in combination with visualization methods. If you want to know more detail about ExonCNV, please see the ExonCNV page.