Advaita Bioinformatics helps principal investigators, core facilities, and enterprise bioinformatics teams analyze gene expression and variant data to find biomarkers, identify impacted pathways, and pinpoint putative mechanisms. Currently, this frustrating process is slow, unreliable, expensive, and often requires multiple disjointed tools, which then provide irrelevant or incorrect results. While other solutions drop a haystack of results on you, we lead you straight to the needle.
Who We Serve
Core Facilities & Service Providers
Service providers face a dilemma. On one hand you want to provide the best service that you can for their customers. On the other hand, frequent requests for changes can take up time without bringing in more revenue. The more you do for customers, the higher their satisfaction, but the less profitable the relationship becomes. You need a way to provide optimal, streamlined service and yet empower your customer to drill down on their own results, thus eliminating requests for re-analysis. This is not easy– it requires power, flexibility, and ease that other solutions simply do not offer.
Enterprise Bioinformatics Teams
You’re tasked with distilling mountains of data into simple, actionable insights for multiple projects, with limited time, people, and money. You need to quickly find the needle in the haystack and deliver it effectively in a way that makes sense to your life science collaborators. But, you don’t have the right tools to do that. You can trust our results because they integrate multiple independent forms of evidence and cleverly use not only the content, but the structure of the information in our knowledgebase. Your team will love the comprehensive capabilities you can give them to efficiently and effectively do their jobs.
You want to provide the very best results possible, yet you lack time, personnel and funds to perform the analysis that would satisfy your needs. You could turn to free software. However, this likely means you are using black-box capabilities and/or outdated data and analytical functionality, with no way to get support. Plus, you often need to weave together multiple packages that do not line up between inputs and outputs, jeopardizing the integrity of your results. This is all compounded by the constant shift in support personnel who often perform the analytical work for you. Once these people have moved on, there is no real audit trail of their work, requiring you to start over to continue their work. This is costly, and wastes time, money, and intellectual energy. You deserve better.
What You Get
Our proprietary analysis pinpoints the impacted pathways, with fewer false positives by considering the position and role of all genes on each pathway, as well as the direction and type of all their interactions.
Get a sophisticated and complete analysis of your experiment at a cost much lower than any other solution, (including “free”) be it do-it-yourself or off-the-shelf.
Get the answers you are looking for while you enjoy a cup of coffee. A complete, multi-dimensional analysis will be ready for you 15 minutes after you upload your data.
According to a recent paper in Nature Methods, most pathway analysis tools are outdated and only capture 25% of the known biological processes and pathways. Our knowledge base is updated regularly to make sure you have the full picture.
High impact journals require excruciating details to ensure results are reproducible. Our software automatically tracks the source and version of each piece of information used in any analysis.
Explore your results in real-time, from anywhere, in a highly secure manner. Share interactive analyses with your collaborators at the click of a button. Print an automatically-generated report including publication-ready figures and results, as well as full methods and references.
Our customers are world-renowned experts who trust us to help solve their toughest problems.
You, too, can be among the elite scientists who rely on us.
Each of our customers uses one or more of the following products to address their individual challenges.
Identify significant pathways
without all the noise found
in other approaches.
Provide systems biology context.
Identify variants and biological
impact in minutes.
Search Advaita’s extensive
knowledge base of over
100 million relationships.