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Frontiers | SECNVs: A Simulator of Copy Number Variants and Whole-Exome Sequences From Reference Genomes
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
inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing - Saowwapark Chanwigoon, Sakkayaphab Piwluang, Duangdao Wichadakul, 2020
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Benchmarking germline CNV calling tools from exome sequencing data. - Abstract - Europe PMC
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inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing - Saowwapark Chanwigoon, Sakkayaphab Piwluang, Duangdao Wichadakul, 2020
VS-CNV Command-Line CNV Tool | The Golden Helix Blog
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
Copy Number Variation Tool
CNV Analysis Shifts Focus to NGS Sequences | Biocompare: The Buyer's Guide for Life Scientists
A) Number of duplications and deletions called by CNV calling tools in... | Download Scientific Diagram
inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing | Semantic Scholar
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Frontiers | SCCNV: A Software Tool for Identifying Copy Number Variation From Single-Cell Whole-Genome Sequencing
The changes of tools' performances with respect to the CNV size. Fig a... | Download Scientific Diagram
A comprehensive benchmark of somatic CNV calling... | Posters | F1000Research
Overview of the pipeline. (1) CNV calling is performed using three... | Download Scientific Diagram
PDF) A tool suite for CNV analysis from exome sequencing data in Galaxy
159 Free Copy Number Variation (CNV) Analysis Tools - Software and Resources
Cancers | Free Full-Text | A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data
Evaluation of CNV detection tools for NGS panel data in genetic diagnostics | European Journal of Human Genetics
