Cancers | Free Full-Text | A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data
CNV Quality Control: tools and guidelines
Comparative study of whole exome sequencing-based copy number variation detection tools | BMC Bioinformatics | Full Text
inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing - Saowwapark Chanwigoon, Sakkayaphab Piwluang, Duangdao Wichadakul, 2020
ClinCNV: multi-sample germline CNV detection in NGS data | bioRxiv
Frontiers | Incorporating CNV analysis improves the yield of exome sequencing for rare monogenic disorders—an important consideration for resource-constrained settings
inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing | Semantic Scholar
A comprehensive benchmark of somatic CNV calling... | Posters | F1000Research
GitHub - mperalc/CNV-resources: Tools to detect CNVs from exome sequencing data
The changes of tools' performances with respect to the CNV size. Fig a... | Download Scientific Diagram
VS-CNV Command-Line CNV Tool | The Golden Helix Blog
A) Number of duplications and deletions called by CNV calling tools in... | Download Scientific Diagram
159 Free Copy Number Variation (CNV) Analysis Tools - Software and Resources
CNV Analysis Shifts Focus to NGS Sequences | Biocompare: The Buyer's Guide for Life Scientists
Benchmarking germline CNV calling tools from exome sequencing data | Scientific Reports
Cancers | Free Full-Text | A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data
Convoy® Super - TAJIMA TOOL
DeAnnCNV
Copy number variant (CNV) detection at Blueprint Genetics - Blueprint Genetics