Berlin, 24.03.2025

We are proud to announce that Lucid Genomics is funded by the European Regional Development Fund (EFRE) supported through the Investitionsbank Berlin (IBB).

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Project name

Development of deep learning technologies for accurate detection of large structural variants

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Project description
With the ProFIT project, Lucid Genomics will further develop deep learning technologies for the accurate detection and analysis of structural variants in short-read whole-genome sequencing data. Short-read sequencing is currently only able to accurately detect single nucleotide variants. Other technologies such as long-read sequencing are too expensive to be used substantially. The AI-Framework that will be developed will enable different types of users to use their data more extensively.