Introduction

Advanced data integration - the answer for an efficient omics data journey. During this session, we will demonstrate how an improved annotation of omics data and the enrichment with public and internal reference data helps to find a relevant subset faster and is a solution to avoid missing out. Performing omics experiments in high throughput has become a common technique in biomedical research.

The growing popularity has been instrumental in major breakthroughs but has some drawbacks too. Omics data often miss 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 really need. In this webinar, we will demonstrate how an improved annotation of omics data and the enrichment with public and internal reference data helps to find a relevant subset faster and is a solution to avoid missing out.

The DISQOVER platform helps you to search, browse and filter the available data. In addition, when DISQOVER is 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.

Speakers

Filip Pattyn

Scientific Advisor

DISQOVER Platform ONTOFORCE

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