Ultra-long-read whole-genome sequencing that detects structural variants, repeat expansions and DNA methylation in a single run. Suited to rare-disease research and complete (T2T) genome assemblies.

The service is being established, with launch planned for 2027. Contact the head of the lab about collaboration or advance booking.

Contact: Dr Oliver Vugrek, Oliver.Vugrek@irb.hr, +385 1 469 8844