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Top 10 Reasons to Choose GenomeQuest
- It Can Vastly Improve Researcher Productivity, Especially for NGS-based Discovery
- A Basic Account is Free
- You Can Be Using and Learning this "New Way" in 5 Minutes
- You Can Configure It to Your Specific Needs
- It Connects to and Hosts Sequence Data Management for Other Discovery Tools
- It Works with All Sequence Machines
- It's Built To Scale to NGS-Level Performance
- It Offers Important Advantages for your Bioinformatics, IT, And Business Managers
- Overall, You and Your Organization will be Equipped to Discover Far Faster
- The Product is Relied Upon by Industry Leaders and has Earned a High Satisfaction Rating
Rapid Annotation Workflow
The GenomeQuest sequence data management platform allows you to analyze next generation sequencing data from any platform (Illumina, SOLiD, 454). This video steps through the Rapid Annotation Workflow for the automatic annotation and analysis of 378K 454-FLX reads. With RAP, you can perform the analysis of metagenomics experiments, assess the purity of your NGS samples, and find new pathogens.