A trustworthy foundation for variant calling
Clinical & Medical Research
WGS / WES variant calling built on nf-core/sarek, supporting germline and somatic analysis with functional annotation — meeting research-grade rigor and traceability.
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Germline / somatic variants
WGS / WES support
Variant functional annotation
Fully traceable
Note: results from this platform are for scientific research only and do not constitute a basis for clinical diagnosis.
A trustworthy foundation for variant calling
WGS / WES variant calling built on nf-core/sarek, supporting germline and somatic analysis with functional annotation — meeting research-grade rigor and traceability.
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