We are excited to be able to offer our customers and registrants this opportunity to experience our integrated suite of genome interpretation products. For the first time, Cytognomix is offering a free trial of our MutationForecaster® genome interpretation suite to all registrants of the product. No subscription is required to analyze data with any of our software tools. Trial users are provided with the same datasets that we have analyzed in our peer-reviewed publications. Start your trial whenever you’re ready.
The trial showcases many capabilities available to subscribers:
- Run all of our major software products with their built-in filters:
- Automated Splice Site and Exon Definition Analysis (ASSEDA)
- Shannon Splicing Mutation Pipeline
- Veridical
- Variant Effect Predictor (VEP)
- Cytognomics Visualization Analytics for literature and genomic validation (CytoVA)
- Cytognomix User Variation Database (CUVD)
2. Customize results with any of these products:
- Alter parameters and change information models in ASSEDA
- Custom filtering of results obtained from the Shannon pipeline, Veridical, and VEP
- Run literature or cytogenomic-based queries of Medline with CytoVA
- Export results to CUVD, which you can search, modify, or analyze variants with a wide variety of external databases then archive results of searches
- Download results from any product
3. Streamline analysis of a dataset with all of these products in a single run using Workflows
Once you see the discoveries that only MutationForecaster® can make, we are confident that you will sign up for a subscription to analyze your own data.
Contact us if you have questions about the trial.
Happy holidays!