Long-Read Sequencing Uppsala, October 31 – November 2, 2022

#LRUA22: Empower your research with long-read sequencing technologies

In recent years, long-read DNA sequencing technologies have 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 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.

National Genomics Infrastructure (NGI)