Webinar Videos
BioDiscovery is pleased to provide copies of previously recorded webinars to customers and colleagues. Webinars will be posted based upon interest and feedback from attendees. If you encounter any problems watching the videos simply emailsupport@biodiscovery.com for assistance.
February 2, 2012 – Integrated Genomic Analysis using Nexus Copy Number Nexus Expression
Integration of genomic data from different modalities (e.g. copy number variation, gene expression, miRNA expression, etc.) is a major area of interest with the growing ability to extract such information using high throughput methods such as microarrays. In this presentation we will highlight how BioDiscovery’s Nexus Copy Number and Nexus Expression software solutions can be used by research scientists to integrate knowledge gain from one modality with another to create a complete picture of the underlying biology. We will use data generated by The Cancer Genome Atlas (TCGA) project on a set of ovarian cancer samples. The data will include copy number and LOH analysis from SNP arrays as well as mRNA and miRNA data generated using microarray technology. We will show how to identify regions of significant copy number change that are predictive of survival and how the expression of the genes in these regions can also be predictive of survival. Time permitting, we will also look at the effect of miRNA expression changes on target gene expression.
Sneak Peak at Nexus Expression 3.0
In this presentation we will demonstrate the power of Nexus Expression in simplifying the process of data exploration and visualization in gene expression data obtained from various array technologies. We will highlight new features in upcoming new version (v. 3.0)…
Simplifying Gene Expression Analysis with Nexus Expression
In this presentation we will demonstrate the power of Nexus Expression in simplifying the process of data exploration and visualization in gene expression data obtained from various array technologies…
Single Sample CNV/LOH Analysis and Visualization with Nexus Solo
In this presentation we will show how to analyze CGH/SNP array data from a single sample to uncover gains/losses, LOH/allelic events, and correlate with data from external databases such as the DGV…
Application of ASCAT Processing to Tumor Samples Using Nexus Copy Number 6
Analyzing copy number variation in cancer tissues can be a difficult task due to the heterogeneity of the cell population. The soon to be released version 6.0 of Nexus Copy Number has a number of new tools that will help address these issues…
Enhanced Data and Result Sharing with Nexus DB Version 6
In this presentation we will cover many new enhancements to Nexus DB that will be part of the version 6 release. These enhancements are designed to offer users more autonomy in creating groups, enhanced controls over data access rights, graphical display of query results and much more…
Cytogenetic Review – Nexus Copy Number 6.0
In this presentation we will demonstrate CNV and LOH analysis tools that will help cytogeneticists speed up their process of reviewing samples and make better decisions on the significance of events being detected . The Nexus Copy Number is a platform independent solution for analysis and visualization of CNV and LOH from CGH and SNP arrays…
Educational Webinar Series: Cancer Survival Analysis with Nexus Copy Number
Please join us for the second presentation in our new educational webinar series where we examine and show how to answer certain biological questions using Nexus Copy Number. This is not a software demo such as a general introduction to Nexus Copy Number software nor is it a demonstration of software features…
Educational Webinar Series: Comparisons Between Array Platforms & Between Different Analysis Methods
Please join us for our inaugural webinar in a new webinar series (Array Data Analysis Tutorials) where we examine and show how to answer certain biological questions using Nexus Copy Number. This is not a software demo such as a general introduction to Nexus Copy Number software or demonstration of software features…
Translating Array & Sequence Based Investigations of Prostate Cancer
The application of aCGH and next generation sequencing technologies to the analysis of prostate tumor genomes and transcriptomes for identification of biomarkers and therapeutic targets will be discussed. Special challenges associated with analyzing NGS and microarray data and their integration with diverse data sets will be discussed…
Application of Nexus Copy Number to the Analysis of TCGA Generated Ovarian Cancer Data
In this webinar we present analysis of ovarian cancer highlighting features such as class comparisons and gene enrichment found in the Discovery Edition of Nexus Copy Number 5.0. We will show how we used the comparisons feature and identified genomic regions consisting of 1049 genes with significant copy number change in samples with progressive disease vs. samples with complete response to therapy…
Nexus Copy Number – Simplifying Copy Number Analysis
Analysis and interpretation of copy number and Loss of Heterozygousity (LOH) data from CGH or SNP arrays can be an overwhelming and time consuming task. With the increase in density of these platforms, many hundreds of potential aberrations can be detected, further increasing the time and complexity of the interpretation process…
Copy Number & LOH Analysis of Esophageal Adenocarcinoma with Nexus Copy Number
In this presentation we utilize data from a recently published paper by Nancarrow et. al (Cancer Research 2008) in which a set of 23 esophageal adenocarcinoma (EAC) primary tumor biopsies were analyzed using Illumina Sentrix HumanHap300 BeadChip arrays…














