Long-Read Sequencing Uppsala 2026

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.

Oxford Nanopore will be exhibiting at LRUA 2026. We will also be hosting a presentation on Day 1 of the conference and a workshop on Day 2.

Speaker and session details will be announced soon.

Please register to reserve your place and don't forget to visit us at our booth.