Performing omics experiments in high throughput has become a common technique in biomedical research. There’s an abundance of omics data but often its difficult to find the subset you really need. DISQOVER improves the annotation of omics data to avoid missing out on relevant subsets.
Challenges in Omics Data Integration
The growing popularity of omics experiments has been instrumental in major breakthroughs, but has some drawbacks too. Omics data often misses proper and consistent metadata and causes a strange paradox.
There’s an abundance of omics data in the public domain or generated within organizations but in many cases it’s difficult to find the subset you are looking for.
A touch of DISQOVER
An improved annotation of omics data and the enrichment with public and internal reference data helps to find a relevant subset faster. As a result, DISQOVER is a solution for an efficient omics data journey and to avoid missing out. In addition, when embedded in a software ecosystem, search results can be used to link-out to downstream applications where a (re-)analysis for the raw data is possible.
Advantages of DISQOVER for Integrated Omics Data
- Make better decisions by creating an efficient omics data journey, thanks to advanced data integration
- Search, browse and filter in all available omics data sets
- Re-ingest raw data from linked downstream applications to find new insights
Try the free Community Edition or upgrade to DISQOVER 6.00 Enterprise
Experience the DISQOVER 6.00 Community Edition right now:
- Create a free account
- Enjoy unlimited action to public data
- Access ~150 data sources
- Create your own dashboards and share them with peers
Contact us to unlock the full DISQOVER experience with the ability to link internal and third-party data sources to create a truly data ecosystem.