The changes of tools' performances with respect to the CNV size. Fig a... | Download Scientific Diagram
PDF) A tool suite for CNV analysis from exome sequencing data in Galaxy
A comprehensive benchmark of somatic CNV calling... | Posters | F1000Research
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inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing - Saowwapark Chanwigoon, Sakkayaphab Piwluang, Duangdao Wichadakul, 2020
Frontiers | Incorporating CNV analysis improves the yield of exome sequencing for rare monogenic disorders—an important consideration for resource-constrained settings
Overview of the pipeline. (1) CNV calling is performed using three... | Download Scientific Diagram
CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencing | Scientific Reports
Frontiers | SECNVs: A Simulator of Copy Number Variants and Whole-Exome Sequences From Reference Genomes
New tools for CNV calling and low-frequency somatic calling · Issue #3322 · bcbio/bcbio-nextgen · GitHub
Visualization of individual-sampled analysis after integrating CNV tool... | Download Scientific Diagram
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
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Comparative study of whole exome sequencing-based copy number variation detection tools | BMC Bioinformatics | Full Text
A) Number of duplications and deletions called by CNV calling tools in... | Download Scientific Diagram
Benchmarking germline CNV calling tools from exome sequencing data | Scientific Reports
GitHub - mperalc/CNV-resources: Tools to detect CNVs from exome sequencing data
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
