Experience CURIO first-hand with no cost or obligation. Using CURIO sample data or your own data, explore the features and capabilities of the platform at your leisure and comfort.
- Max 400 Million Reads
Provide us with a FASTQ file not to exceed 400 million reads for upload into CURIO. CURIO data is also available.
- 14 Days Free Access
Get 14 days of free CURIO access for yourself and any 2 other designated team members. CURIO makes sharing and collaborating easy!
- 30-Minute Intro Session
In order to make sure your experience is a great one, we will provide a 30-minute introductory session to highlight the features and capabilities of CURIO.
*No Payment Required
Provide your contact details below, and we will respond back within 1 business day to begin your free access setup.
Transitioning to NGS has become less a matter of sequencing costs and more about how to manage, analyze, and operationalize the massive amount of data generated by NGS. CURIO turns this potential bioinformatics bottleneck into your competitive advantage.
Transitioning to NGS has become less a matter of sequencing costs and more about how to manage, analyze, and operationalize the massive amount of data generated by NGS. CURIO turns this potential bioinformatics bottleneck into your competitive advantage.
CURIO is a breeder-friendly bioinformatics platform that transforms sample data in valuable insights that lead to better breeding decisions.
- Data Management
NGS generates massive volumes of complex genomic data that can overwhelm traditional analysis workflows and storage systems.
CURIO quickly aligns raw sample data and automatically organizes this data into intuitive project structures, keeping everything neat, accessible, and usable.
- Data Analysis
Translating complex genomic data requires bioinformatics expertise not readily available to most breeders.
CURIO was designed to put the power of advanced bioinformatics into the hands of non-bioinformaticians through its intuitive point-and-click user interface, real-time visualizations, and ease of analysis configuration.
- Workflow Integration
Concern over losing continuity with existing datasets and established breeding program workflows.
CURIO is a single system to analyze legacy data as well as new NGS data. With its flexible workflow capabilities, CURIO provides a seamless transition to NGS, even for complex integrations including automation.
- Data Management
NGS generates massive volumes of complex genomic data that can overwhelm traditional analysis workflows and storage systems.
CURIO quickly aligns raw sample data and automatically organizes this data into intuitive project structures, keeping everything neat, accessible, and usable.
- Data Analysis
Translating complex genomic data requires bioinformatics expertise not readily available to most breeders.
CURIO was designed to put the power of advanced bioinformatics into the hands of non-bioinformaticians through its intuitive point-and-click user interface, real-time visualizations, and ease of analysis configuration.
- Workflow Integration
Concern over losing continuity with existing datasets and established breeding program workflows.
CURIO is a single system to analyze legacy data as well as new NGS data. With its flexible workflow capabilities, CURIO provides a seamless transition to NGS, even for complex integrations including automation.