About GenoSeq

Reproducible genomics for everyone.

We started GenoSeq in 2021 after watching too many research groups rebuild the same ad-hoc pipelines, lose weeks to cluster maintenance, and struggle to reproduce their own results. We believed bioinformatics infrastructure should be a solved problem.

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Our mission

Remove the engineering burden from genomics so biologists can spend their time on biology. Every feature we ship is measured against one question: does it make a research workflow faster, cheaper, or more reproducible?

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Who we serve

Academic cores, clinical research labs, agrigenomics teams, and biotech startups across 38 countries โ€” from solo PIs running their first pipeline to consortia processing thousands of samples a week.

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Open by default

We build on open-source tools โ€” BWA, minimap2, SAMtools, GATK, DeepVariant โ€” and contribute back. Our reference workflows are published under a permissive license.

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By the numbers

4,100+ active labs, 2.4 petabases processed, and a 99.98% pipeline uptime SLA. We publish a quarterly transparency report on our operations.

Leadership

A team of genomics researchers, distributed-systems engineers, and bioinformaticians.

Dr. Lena Hartmann

Co-founder & CEO. Formerly lead of the comparative genomics core at a major research institute.

Ravi Subramanian

Co-founder & CTO. Built large-scale workflow schedulers at a cloud hyperscaler.

Dr. Mei Tanaka

Head of Science. Population geneticist focused on variant-calling accuracy.

Want to work with us?

We're hiring across engineering, science, and product. Remote-friendly, with hubs in Cambridge and Berlin.

See open roles