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
Clinical Genomics Uppsala

Gold Sponsors

Oxford Nanopore Technologies

Silver sponsors

New England Biolabs
Twist Bioscience
Nordic Biosite
Zymo Research

Bronze Sponsors

10X Genomics
Sage Science


Academic Conferences - the conference administration office
Phone: +46 18 671533 or +46 18 671003
E-mail: LRUA22@akademikonferens.se


Important dates

Sept 11, 2022    Abstract submission deadline
Sept 16, 2022    Abstract notification message
Oct 11, 2022      Early bird registration deadline - extended


Organized by

National Genomics Infrastructure (NGI)