Nexus Copy Number 10.0

Nexus Copy Number is a powerful and user-friendly application from BioDiscovery that equips researchers with advanced genome analysis and data mapping tools. This program provides the ultimate in statistical tools for advanced scientific exploration so that it is easy for the user to use. The program uses aCGH, SNP array, and NGS data to examine DNA variability, and also allows the user to detect missing or amplified pieces of DNA or alteration of allelic events.

This software is a multi-faceted desktop application for detecting genomic transformations. The program accepts data from various manufacturers such as Infinium GSA and CytoScan XON.

Features and specifications of Nexus Copy Number software:

Collaborative event detection, enriched analysis and categorization

Comparison between genomes to detect statistically significant differences

Analyze and visualize multiple samples in parallel – without the need for any bioinformatics expertise

Integrate mRNA and miRNA strands, methylate and copy number changes to detect genome hotspots

Search for regions / genes among various GEO and TGGA projects using Nexus DB repositories

Integration of phenotypes and genomic data to reveal significant correlations

required system

It is recommended to increase the memory allocated to the Multiscale BAM Reference Builder to about 50% of total memory available; at minimum the reference builder requires 4GB of memory.