BioDiscovery

Nexus Copy Number™

Version 10.0 has the next generation MSR algorithm for deriving copy number and allelic events from NGS data. The enhanced algorithm is optimized for NGS panel data where coverage across the genome is uneven, allowing the software to perform well on a variety of NGS data (WES, WGS, tageted panel, and shallow sequencing). Learn more.

Why Choose Nexus Copy Number?

Demo | Features & Benefits | Resources

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).

Nexus Copy Number 10.0 enhanced algorithm is optimized for NGS panel data where coverage across the genome is uneven, allowing the software to perform well on a variety of NGS data (WES, WGS, tageted panel, and shallow sequencing).Learn more.

Features & Benefits

Identification of cooperating events, enrichment analysis, and clustering

Comparisons between genomic profiles to identify statistically significant differences

Analysis and visualization of multiple samples in parallel – no bioinformatics expertise required

Supports data from Affymetrix, Agilent, Illumina, OGT, etc.

Detection of copy number from aCGH and SNP arrays

Copy number and BAF estimation from NGS (WGS, WES, targeted panels)

Integration of mRNA, miRNA, sequence variants, methylation and copy number changes to identify genomic hotspots

Query for region/gene across multiple projects from GEO and TCGA via Nexus DB repository

Integrate phenotypic and genomic data to uncover significant correlations

Request a demo to try the software yourself

Install Nexus Copy Number demo and start your data

Need help? BioDiscovery Support is only a call/email away

Go from Raw Data to Advanced Analysis in Minutes!

Get Started Today by Downloading a Free Trial.

System Requirements:
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

BioDiscovery Benefits

Versatility

Able to handle and process data from all commercial platforms.

Efficiency

Optimum usage of computing.

Acute Sense of Fitness for Purpose

Usefulness to our community of users.

These products empower Biologists and Geneticists with sophisticated, yet highly usable tools to analyze and interpret their data and draw meaningful conclusions.