Your browser doesn't support javascript. This means that the content or functionality of our website will be limited or unavailable. If you need more information about Vinnova, please contact us.

LockSeq - Enabling Routine and Streamlined gene editing outcome characterization for cell & gene therapy development and validation

Reference number
Coordinator Countagen AB
Funding from Vinnova SEK 500 000
Project duration October 2025 - May 2026
Status Completed
Venture Innovative Startups
Call Innovative Startups 2025

Important results from the project

All project goals were met, and several were exceeded. Detection sensitivity reached <1:1,000 ten times better than the 1:100 target. five pilot studies were completed with the nist genome editing consortium and the genehumdi cost network turnaround time fell by more than 50 and wp2 customer interviews produced an improved pricing model. lockseq is now commercialized with its first paying customers onboard.>

Expected long term effects

The results strengthen LockSeq´s position in gene editing outcome characterization. The commercial launch and first customer agreements support both a follow-on grant applications and an ongoing external financing round.

Approach and implementation

The project ran in two work packages as planned: WP1 (Oct 28, 2025–Feb 28, 2026) with five pilot studies through the NIST Genome Editing Consortium and GeneHumDi COST network, followed by WP2 (Mar 2–May 1, 2026) with more than 20 customer interviews to develop the business model and pricing strategy.

External links

The project description has been provided by the project members themselves and the text has not been looked at by our editors.

Last updated 26 June 2026

Reference number 2025-02204