Cancers | Free Full-Text | A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data
Frontiers | Incorporating CNV analysis improves the yield of exome sequencing for rare monogenic disorders—an important consideration for resource-constrained settings
PDF) A tool suite for CNV analysis from exome sequencing data in Galaxy
DeAnnCNV
Frontiers | SCCNV: A Software Tool for Identifying Copy Number Variation From Single-Cell Whole-Genome Sequencing
Cancers | Free Full-Text | A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data
Copy Number Variation Tool
inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing - Saowwapark Chanwigoon, Sakkayaphab Piwluang, Duangdao Wichadakul, 2020
Evaluation of CNV detection tools for NGS panel data in genetic diagnostics | European Journal of Human Genetics
Benchmarking germline CNV calling tools from exome sequencing data | Scientific Reports
A) Number of duplications and deletions called by CNV calling tools in... | Download Scientific Diagram
CNV Quality Control: tools and guidelines
PennCNV-Affy - PennCNV
Overview of the pipeline. (1) CNV calling is performed using three... | Download Scientific Diagram
TAJIMA CNV-J900SP Caulk Gun - 14 Gallon 1 Quart France | Ubuy
VS-CNV Command-Line CNV Tool | The Golden Helix Blog
A comprehensive benchmark of somatic CNV calling... | Posters | F1000Research
ClinCNV: multi-sample germline CNV detection in NGS data | bioRxiv
Benchmarking germline CNV calling tools from exome sequencing data. - Abstract - Europe PMC
Comparative study of whole exome sequencing-based copy number variation detection tools | BMC Bioinformatics | Full Text
New tools for CNV calling and low-frequency somatic calling · Issue #3322 · bcbio/bcbio-nextgen · GitHub
inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing | Semantic Scholar
Cancers | Free Full-Text | A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data
159 Free Copy Number Variation (CNV) Analysis Tools - Software and Resources
