PDF) A tool suite for CNV analysis from exome sequencing data in Galaxy
Comparative study of whole exome sequencing-based copy number variation detection tools | BMC Bioinformatics | Full Text
Cancers | Free Full-Text | A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data
Benchmarking germline CNV calling tools from exome sequencing data. - Abstract - Europe PMC
CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencing | Scientific Reports
The changes of tools' performances with respect to the CNV size. Fig a... | Download Scientific Diagram
Convoy® Super - TAJIMA TOOL
A) Number of duplications and deletions called by CNV calling tools in... | Download Scientific Diagram
Cancers | Free Full-Text | A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data
PennCNV-Affy - PennCNV
Overview of the pipeline. (1) CNV calling is performed using three... | Download Scientific Diagram
GitHub - mperalc/CNV-resources: Tools to detect CNVs from exome sequencing data
Convoy® Lite - TAJIMA TOOL
VS-CNV Command-Line CNV Tool | The Golden Helix Blog
Comparative study of whole exome sequencing-based copy number variation detection tools | BMC Bioinformatics | Full Text
DeAnnCNV
Cancers | Free Full-Text | A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data
Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms | BMC Bioinformatics | Full Text
Copy Number Variation Tool
inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing - Saowwapark Chanwigoon, Sakkayaphab Piwluang, Duangdao Wichadakul, 2020
CNV Quality Control: tools and guidelines
inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing | Semantic Scholar
Frontiers | Incorporating CNV analysis improves the yield of exome sequencing for rare monogenic disorders—an important consideration for resource-constrained settings
Frontiers | SCCNV: A Software Tool for Identifying Copy Number Variation From Single-Cell Whole-Genome Sequencing
Visualization of individual-sampled analysis after integrating CNV tool... | Download Scientific Diagram
