Long-Read Sequencing

#LRUA22 Empower your research with long-read sequencing technologies

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

Interested? Register here

Questions? LRUA22@akademikonferens.se


SciLifeLab Uppsala
Entrance C11, BMC
Husargatan 3
752 37

Date / Time

2022-10-31 - 2022-11-02

08:30 - 12:00

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