Frontiers | SCCNV: A Software Tool for Identifying Copy Number Variation From Single-Cell Whole-Genome Sequencing
Frontiers | Incorporating CNV analysis improves the yield of exome sequencing for rare monogenic disorders—an important consideration for resource-constrained settings
Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms | BMC Bioinformatics | Full Text
inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing - Saowwapark Chanwigoon, Sakkayaphab Piwluang, Duangdao Wichadakul, 2020
PennCNV-Affy - PennCNV
New CNV Tools with VarSeq 2.2.2 Update | The Golden Helix Blog
DeAnnCNV
ClinCNV: multi-sample germline CNV detection in NGS data | bioRxiv
Convoy® Super - TAJIMA TOOL
Benchmarking germline CNV calling tools from exome sequencing data. - Abstract - Europe PMC
Benchmarking germline CNV calling tools from exome sequencing data | Scientific Reports