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Biodiscovery Nexus Software
Nexus Copy Number is a multifaceted desktop software for rapid discovery of genomic alterations. The interactive visualization and powerful statistical tools allow detection of structural variations (e.g. copy number, homozygous regions), association with sequence variations (point mutations, InDels, inversions, etc.), and identification of statistically significant co-occurring up/down regulated genes (from mRNA, miRNA, and RNASeq data).
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Nexus Copy Number – Accelerating Copy Number Analysis Research (link is external)
Nexus Copy Number simplifies genetic aberration analysis with an elegant and simple user interface, efficient processing for rapid and automated analysis of thousands of arrays. It has a flexible design that accommodates user preferences such as custom annotation tracks, integration of custom databases (e.g. CNVs, genetic disorders), segmentation algorithm, and integration of miRNA and gene expression data. With detection of copy number and LOH events and flexibility in handling any commercial or custom array as well as any organism, Nexus Copy Number is the only solution you need for array based genetic aberration analysis.
Installation on an NIH-issued computer (desktop/laptop) requires administrative privileges.
32-bit Platforms Supported: Windows Win7/8/10 • Minimum: 2 GB RAM • Recommended: 4 GB RAM
64-bit Platforms Supported: Windows Win7/8/10 / OSX / Linux • Minimum: 4 GB RAM • Recommended: 8 GB RAM
This is an NCI-licensed software based on a limited concurrent use license. Access may be limited on the number of users at any given time. NCI will periodically adjust the licensing based on usage.
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