In recent years, long-read DNA sequencing technologies have continued to mature and have now replaced short-read sequencing as the gold standard solution for a wide range of genomics applications. In addition to producing high quality de novo genome assembly, long-read technologies can also be used to study complex structural variation, full-length RNA isoforms, and epigenetic signals at a completely new level of resolution. 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 in April 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 NGI personnel and company representatives.