Nexus Testimonials

"I feel as though BioDiscovery’s Nexus CGH software puts me back at the bench. It is truly empowering."
Dr. Colin Collins, UC San Francisco

"We have been running several different high density genome-wide arrays in our patient samples, and find that Nexus is the most user-friendly and flexible software we have used to be able to integrate and visualize all of our datasets in one place. We are able to quickly and easily identify key regions of interest and jump straight to relevant statistical tests and bioinformatics tools, making the whole process much more efficient."
Dr. Anjene Addington, Child Psychiatry Branch, NIMH, NIH

"Nexus has allowed us to perform group-wise aCGH analysis much faster and more efficiently than had previously been the case. Nexus is also very easy to use, unlike some other analysis programs, making it accessible to people with less computing prowess. I would not hesitate to recommend the use of this software."
Darren Marjenberg, University of Dundee

"Nexus-CGH has allowed us to analyze over 2,000 samples of high-density snp
array data in a relatively quick and efficient manner. In addition, the
output allows us to quickly identify and visualize regions where copy-number
variants are shared within the population."
Dr. Kurt Hetrick, Center for Inherited Disease Research, Johns Hopkins University

"Our research laboratory is using a wide variety of array CGH platforms and analysis software. We have found NEXUS CGH to be very user-friendly and capable of handling a large number of datasets, simultaneously."
Dr. Charles Lee of Harvard Medical School

"Using NEXUS CGH, my lab has been able to quickly and confidently process large amounts of high-density array CGH data obtained from FFPE tumor samples to identify important chromosomal regions" said Dr. Jeff Gregg head of Molecular Pathology at UC Davis. "NEXUS CGH has allowed us to move from raw data into exploring CNV's and associated genes in a matter of few hours whereas this process might have taken months to complete with other commercial or academic packages.

"We have been using Nexus for the past six months to explore chromosomal loss data in glioblastomas and meningiomas. My lab members have found the tools and visualizations now possible in Nexus Copy Number to greatly accelerate their exploration of the datasets and drill down to interesting individual genes and gain insights that were quite difficult previously.” said Dr. Stanley Nelson, Director, UCLA Site of the NIH Neuroscience Microarray Consortium. “We are excited about the new release which expands and builds on the Nexus platform for greater flexibility and more powerful analyses.  Thanks for creating a very useful product!"

"Nexus has provided us with a powerful tool for rapidly analyzing genome copy number profiles from large datasets using a variety of different platforms and the ability to incorporate expression data. These analyses are permitting us to link genomic and transcriptomic changes to clinical phenotypes and sub-populations.”
Simon Gregory, Assistant Professor at Duke Center for Human Genetics

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