An analysis foundation for genetic variation
Medical research
Use Sarek for germline or somatic variant studies with WGS / WES data. Retain analysis inputs, parameters and outputs for your team to review and reuse.
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Germline and somatic variants
WGS / WES data
Reference data and run settings
Download and reuse analysis results
Note: results from this platform are for scientific research only and do not constitute a basis for clinical diagnosis.
An analysis foundation for genetic variation
Start with Sarek, select samples, reference data and variant analysis steps, then download the generated results.
Data, analyses and reports in one workspace
Start with your next analysis
Choose a built-in analysis, add data, and review the run settings. Bring an existing Nextflow project through the import path.