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Frontiers | Incorporating CNV analysis improves the yield of exome sequencing for rare monogenic disorders—an important consideration for resource-constrained settings
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Frontiers | SCCNV: A Software Tool for Identifying Copy Number Variation From Single-Cell Whole-Genome Sequencing
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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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inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing - Saowwapark Chanwigoon, Sakkayaphab Piwluang, Duangdao Wichadakul, 2020
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Evaluation of CNV detection tools for NGS panel data in genetic diagnostics | European Journal of Human Genetics
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A) Number of duplications and deletions called by CNV calling tools in... | Download Scientific Diagram
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New tools for CNV calling and low-frequency somatic calling · Issue #3322 · bcbio/bcbio-nextgen · GitHub
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inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing | Semantic Scholar
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