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2/6/2021
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Nexus Copy Number is a powerful and user-friendly program from BioDiscovery that equips researchers with advanced genome analysis and data mapping tools. This program provides the ultimate statistical tool for advanced scientific discoveries 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 identify parts of DNA that are missing or amplified, or changes in allelic events.
This software is a multifaceted desktop application for detecting genomic transformations. The program accepts data from various manufacturers such as Infinium GSA and CytoScan XON.
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 between different GEO and TGGA projects using Nexus DB repositories
Integrate phenotypes and genomic data to reveal significant correlations
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.
In the Readme file in the Crack folder.
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