- Basic Linux usage
- NGS read-to-reference alignment (genomic and RNA-Seq)
- Variant calling in populations
- De novo assembly of RNA-sequence data
- RNA-Seq expression analysis
Analysis techniques covered will focus mostly on data from the Illumina platform, but we will discuss other sequencing platforms and the advantages and challenges to using their data.
Course fee: 1800 SEK
Application dead-line: 17 August
The course will be held in Uppsala
Link to application form (via SciLife Lab)
For more information, please contact Eva Molin, firstname.lastname@example.org.
If you are admitted to the course (after applying via SciLifeLab above) you can apply for co-funding of travel/accommodation for participating in the course by filling out the form below. No co-funding is provided with respect to the course fee.
Bookings are closed for this event.