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
Convoy® Super - TAJIMA TOOL
Copy number variant (CNV) detection at Blueprint Genetics - Blueprint Genetics
CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencing | Scientific Reports
inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing - Saowwapark Chanwigoon, Sakkayaphab Piwluang, Duangdao Wichadakul, 2020
New CNV Tools with VarSeq 2.2.2 Update | The Golden Helix Blog
Benchmarking germline CNV calling tools from exome sequencing data. - Abstract - Europe PMC
New tools for CNV calling and low-frequency somatic calling · Issue #3322 · bcbio/bcbio-nextgen · GitHub
PDF) A tool suite for CNV analysis from exome sequencing data in Galaxy
A) Number of duplications and deletions called by CNV calling tools in... | Download Scientific Diagram
Comparative study of whole exome sequencing-based copy number variation detection tools | BMC Bioinformatics | Full Text
The changes of tools' performances with respect to the CNV size. Fig a... | Download Scientific Diagram
Evaluation of CNV detection tools for NGS panel data in genetic diagnostics | European Journal of Human Genetics
Frontiers | Incorporating CNV analysis improves the yield of exome sequencing for rare monogenic disorders—an important consideration for resource-constrained settings
Comparative study of whole exome sequencing-based copy number variation detection tools | BMC Bioinformatics | Full Text
Frontiers | SECNVs: A Simulator of Copy Number Variants and Whole-Exome Sequences From Reference Genomes
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
ClinCNV: multi-sample germline CNV detection in NGS data | bioRxiv
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
DeAnnCNV
CNV Analysis Shifts Focus to NGS Sequences | Biocompare: The Buyer's Guide for Life Scientists
VS-CNV Command-Line CNV Tool | The Golden Helix Blog
GitHub - mperalc/CNV-resources: Tools to detect CNVs from exome sequencing data
