You can use the power of Intrepid Bioinformatics to get the most use out of your data, whether you’re working with NGS data, SNP microarrays, assays, or other DNA sequencing-related data. Using our interface, you can choose to upload individual data sets through a simple drag-and-drop method that will quickly upload your data, parse it so that it is organized and accessible, and immediately viewable through our genome browser or accessible programmatically through the open API. All of this is done safely and securely so that no unauthorized users have access to your data. Data sets too large for internet speeds can also be mailed on hard drives.

Collaboration tools built into the system allow you to quickly, securely share your data with other users, eliminating the need to email files, ship hard drives, or sort through old files and misplaced data.

Once data has been uploaded, you have access to it immediately in order to compare it to the reference genome, check allele and genotype frequencies, view repeats, polymorphisms, genotype counts, and more. Maintaining all your data in one location will allow you to easily streamline your work so you can focus on publishing papers, acquiring grants, completing your research, and sharing your data (if you choose to do so). There’s no need to manage a series of hard drives or deal with servers and data centers. Just log into your account and everything you need is at your fingertips.

We encourage you to check out the Gene Browser for free to see just one of the features we offer to help you in your work. If you are interested in learning more, we’d love to hear from you. You can email us at