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GenoLogics | LIMS Story & Exit to Illumina | Listwin Ventures

The GenoLogics story: a laboratory information management platform for genomics labs, plus Don Listwin’s investment perspective and Illumina exit context.

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Full-stack LIMS

Role-based dashboards and API hooks kept wet-lab teams, bioinformaticians, and leadership in sync without forcing custom software builds.

Clinic-ready compliance

Configurable SOP templating, audit trails, and validation tooling let CLIA/CAP labs move from pilot studies to regulated diagnostics faster.

Acquirer integration

Bringing GenoLogics into Illumina ensured new chemistries and automation hardware shipped with cloud workflows that were proven in the field.

References

Related reading

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Interview

Teradici (HP Anyware) • Aug 10, 2016

Inside Teradici: Getting to Know Don Listwin, Chairman

Q&A with Don Listwin on leadership, cloud computing, and his investment perspective in networking and software.

Momentum

A timeline from lab benches to Illumina

GenoLogics scaled with the exact needs of translational researchers, ending with an acquisition that made Illumina’s workflows even more turnkey for hospital-grade programs.

2003–2005

Origins in proteomics labs

GenoLogics built configurable lab information management software (LIMS) so translational researchers could tie together instruments, SOPs, and growing volumes of proteomics data.

2006–2010

NGS acceleration

Next-generation sequencing took off and the platform evolved to coordinate sample prep, run planning, and QC reporting so research hospitals could scale their programs.

2012–2015

Acquisition by Illumina

Illumina acquired GenoLogics in 2015 to deliver tighter workflows between the sequencer hardware, BaseSpace, and the labs driving precision-medicine advances.

Why it matters now

Precision-medicine labs still need builders

GenoLogics validated Don’s thesis: pairing disciplined software operators with bioengineering unlocks durable value. If you are building the next LIMS, diagnostics workflow, or data router for clinical genomics, reach out.