LRUA26

Long-Read Sequencing Uppsala, 2026

#LRUA26: Empower your research with long-read sequencing technologies

Long-read sequencing technologies are replacing short-read sequencing as the gold standard solution for a wide range of genomics applications. In addition to producing high quality de novo genome assemblies, long-read technologies can be used to study complex structural variation, full-length RNA isoforms, detection of epigenetic signals, and much more. The adaptation of long-read sequencing is sweeping through several areas of the life sciences including agricultural, environmental, and medical research.

Join us in Uppsala to catch up with the latest developments in long-read sequencing technologies and their applications, get inspired by peers presenting their research, and enjoy discussions with leading experts and company representatives.

Organizers

Main organizer: National Genomics Infrastructure
Co-organizer: Clinical Genomics Uppsala
Co-organizer: The Long-Read Transcriptomics European Consortium

Contact

Academic Conferences - the conference administration office
Phone: +46 18 671533 or +46 18 671003
Email: LRUA26@akademikonferens.se

 

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Important dates

TBA

Organized by

National Genomics Infrastructure (NGI)

Clinical Genomics Uppsala (CGU)