Technical spotlight: Detecting small- and medium-length copy number variants by whole-genome sequencing
![](https://www.illumina.com/content/dam/illumina-marketing/images/genomics-research/articles/small-cnv-calling/Small%20CNV%20calling_table1.png)
Historically, detecting different sizes of genetic variants has required using multiple different tests. By combining Illumina WGS with secondary analysis algorithms built into the DRAGEN Bio-IT Platform, researchers can achieve high-sensitivity detection of all these different variant types using a mixture of methods described here.
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FlowCNV-seq: an almost novel metthod for single-cell copy number analysis - Enseqlopedia
![](https://www.illumina.com/content/dam/illumina-marketing/images/company/featured-articles/FUJI.jpg)
Copy Number Variation (CNV) Analysis
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GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data
![](https://www.biorxiv.org/content/biorxiv/early/2019/11/22/847681/F1.large.jpg)
Robust foreground detection in somatic copy number data
![](https://developer-blogs.nvidia.com/wp-content/uploads/2023/03/parabricks-4-1-featured.png)
Long-Read Sequencing Workflows and Higher Throughputs in NVIDIA Parabricks 4.1
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Detection of chromosome structural variation by targeted next-generation sequencing and a deep learning application
![](https://assets.illumina.com/content/dam/illumina-marketing/images/genomics-research/articles/small-cnv-calling/Small%20CNV%20calling_thumbnail.png)
Technical spotlight: Detecting small- and medium-length copy
![](https://www.illumina.com/content/dam/illumina-marketing/images/genomics-research/articles/small-cnv-calling/Small%20CNV%20calling_table1.png)
Technical spotlight: Detecting small- and medium-length copy number variants by whole-genome sequencing
![](https://www.mdpi.com/cancers/cancers-13-06283/article_deploy/html/images/cancers-13-06283-g003.png)
Cancers, Free Full-Text
London Calling 2021: Day 2
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Considerations for development of gene-edited PSC-based therapies