Offering simple yet powerful tools for CNV analysis and visualization from aCGH, SNP array and NGS data.
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).
The new version allows users without bioinformatics expertise, to easily import BAM files to visualize/analyze copy number as well as LOH and allelic Imbalance events. Learn more.
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Able to handle and process data from all commercial platforms.
Optimum usage of computing.
Usefulness to our community of users.