300048 UE Sequencing bioinformatics for beginners (2026S)
Continuous assessment of course work
Labels
Registration/Deregistration
Note: The time of your registration within the registration period has no effect on the allocation of places (no first come, first served).
- Registration is open from Th 12.02.2026 14:00 to Th 26.02.2026 18:00
- Deregistration possible until Su 15.03.2026 18:00
Details
max. 20 participants
Language: English
Lecturers
Classes (iCal) - next class is marked with N
- Thursday 05.03. 15:00 - 16:30 Seminarraum 1.8, Biologie Djerassiplatz 1, 1.007, Ebene 1
- Thursday 19.03. 15:00 - 16:30 Seminarraum 1.8, Biologie Djerassiplatz 1, 1.007, Ebene 1
- Thursday 26.03. 15:00 - 16:30 Seminarraum 1.8, Biologie Djerassiplatz 1, 1.007, Ebene 1
- Thursday 16.04. 15:00 - 16:30 Seminarraum 1.8, Biologie Djerassiplatz 1, 1.007, Ebene 1
- Thursday 23.04. 15:00 - 16:30 Seminarraum 1.8, Biologie Djerassiplatz 1, 1.007, Ebene 1
- Thursday 30.04. 15:00 - 16:30 Seminarraum 1.8, Biologie Djerassiplatz 1, 1.007, Ebene 1
- Thursday 07.05. 15:00 - 16:30 Seminarraum 1.8, Biologie Djerassiplatz 1, 1.007, Ebene 1
- Thursday 21.05. 15:00 - 16:30 Seminarraum 1.8, Biologie Djerassiplatz 1, 1.007, Ebene 1
- Thursday 28.05. 15:00 - 16:30 Seminarraum 1.8, Biologie Djerassiplatz 1, 1.007, Ebene 1
- Thursday 11.06. 15:00 - 16:30 Seminarraum 1.8, Biologie Djerassiplatz 1, 1.007, Ebene 1
- N Thursday 18.06. 15:00 - 16:30 Seminarraum 1.8, Biologie Djerassiplatz 1, 1.007, Ebene 1
- Thursday 25.06. 15:00 - 16:30 Seminarraum 1.8, Biologie Djerassiplatz 1, 1.007, Ebene 1
Information
Aims, contents and method of the course
Assessment and permitted materials
Active contribution. Solving of 4 challenges during the course (with guidance).
Minimum requirements and assessment criteria
Submission of possible solutions for 4 challenges through Moodle. First, the basic understanding of the approach is evaluated, then the correctness of the solution. Each challenge represents 25% of the mark.
Examination topics
Application of bash commands introduced in the course; application of mapping, genotyping & filtering tools.
Reading list
Association in the course directory
BAN 5
Last modified: Fr 20.02.2026 11:48
How to use the command line? How to work with bash and integrated tools, and using R for analysis and visualization? How to work with big data files, in particular from DNA sequencing? Which file types are used in this context? How to use reference genomes, how to map and filter sequencing data? How to get genotypes, and how to process these?