OES

OES

De-risk omics analysis outcomes

The Omics Engine Service (OES) is a discovery and curation platform for researchers who need ML-ready, curated and standardized omics data to enable their next discovery.

The problem
Public omics data discovery and curation are time‑consuming and cumbersome tasks. Raw omics data are heterogeneous, non-standardized, have limited metadata information and are scattered across the web. Scientists have to manually curate datasets and metadata files to ensure their provenance, completeness and consistency.
The solution
OES catalogs omics raw data and curates their metadata in a standardized, high-resolution, and analysis-ready format so you can leverage the right data for your indication experiments. Bioinformaticians and scientists can quickly search for and download data via an API at three curation depths; raw, basic and premium.
1750+

Curated Samples

250+

Datasets

10+

Omics types

450+

Publications
& BioProjects

High quality omics metadata at your fingertips

With OES, researchers have the flexibility and efficiency gains they need to identify candidate leads in a timely fashion, without compromising the quality or accuracy of their analyses.

This streamlined approach enables scientists to focus on generating insights, rather than laboriously curating omics datasets.

Built by scientists. For scientists.

IT TAKES ONE TO KNOW ONE

OES was born from our need to have access to high quality data for internal and client projects where indication and candidate lead generation was the goal.

HIGH QUALITY, UP-TO-DATE DATA YOU CAN TRUST

OES is an enterprise-level solution that makes sure that you have the latest and greatest of public data for any given health condition.

Through automated pipelines, monthly updates, and manual quality control – supported by internally developed workbench tools for our biocurators – we offer the data universe of interest for further downstream analysis.

What can OES do for you?

Features and Benefits
Reduce curation time by +75%

Focus your time and effort on what truly matters
For health conditions currently available in OES, you can access in minutes quality datasets and metadata that would normally take experts months to curate. No more time, effort and cost wasted on wrangling heterogeneous and messy data of dubious quality.

Use consistent, quality data every time

FAIR-standardized data to enable your next discovery
When it comes to data, quality trumps quantity. And while there is a plethora of public data available, less than 20% is of sufficient quality and compatible for integration. The wrong integration effort can lead to massive time and opportunity costs with high stakes. Through OES you can always access up-to-date, standardized data ready for downstream analysis.

Choose the right curation depth for you

Tap into unparalleled metadata granularity
OES offers three curation depth types for omics data, raw datasets without standardized metadata, basic curation data including general information about samples and files, and premium curation with details reflecting data quality, consistency and how to process. In case the available curation level for a condition is not sufficient for your needs, our dedicated team of biocurators provide custom, high-precision curation with details such as comorbidity status, post-treatment status, unique sample categorization and more.

Bring your own data to OES

Get the most out of integrated datasets
Maximize the value of proprietary data to propel early research and discovery in your organization.
With OES we can integrate your proprietary datasets with publicly curated datasets with the highest quality standards accessible only by you.

Accelerate discovery and de-risk experiments

OES – LEAP™ INTEGRATION

Take your analysis’ insights further

Your omics analysis can only tell you so much about the underlying molecular connections implicated in health and disease. This is where AI can help.

Unlock insights with LEAP™, our AI scientific discovery app

LEAP™ integrates a plethora of public data, over 28 million scientific papers & abstracts, 60+ knowledge bases, clinical trials, and bioinformatics data into a single knowledge graph of 281M known and predicted connections.
Your OES-supported analysis can be automatically integrated to identify additional evidence, novel indications, and guide your design experiments in an optimal way.

Take the hassle out of manual data curation

Reach out to learn how the Omics Engine Service can help your team reduce costs, effort and time by automating omics data discovery and curation.

Request a personalized LEAP™ demo to explore its suitability for your specific R&D priorities.
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