Genomics & Transcriptomics

Course content

The course focuses on sequencing technology, its wide applications, and the Bioinformatics analysis of produced sequencing data. Strategies for analyzing sequencing data will be covered, from preprocessing of raw sequencing data to downstream data analyses. Downstream analyses will be performed using UNIX command tools and R, and will include gene/transcript expression quantification and differential expression analysis from RNA sequencing data and variant/genotype calling from whole-genome DNA sequencing data.

Education

BSc Programme in Bioinformatics 

Learning outcome

Knowledge:

  • Second generation sequencing technology and newer developments
  • Single cell technologies
  • Applications of sequencing technology
    • Overview of how sequencing can be used / adapted to answer various biological questions
  • Analysis strategies and workflows for sequencing data, including
    • Filtering and quality evaluation of raw reads
    • Mapping of sequencing reads
    • Variant and genotype calling from whole-genome DNA sequencing data
    • Gene/transcript expression quantification and differential expression analysis using RNA sequencing data
  • Basic knowledge of the various statistical/​computational approaches and tools used when dealing with sequencing data and how and why these differ between sequencing applications
  • Basic knowledge of the issues and potential problems with sequencing data and how to deal with those
  • Basic knowledge of the impact of study designs and how to avoid and deal with batch effects 
  • Genomic annotation and genome browsers
     

Skills:

  • Analytical strategies of sequencing data
  • Identify differentially expression of gene transcripts between biological samples of different types or conditions
  • Identify mutations in an experimental sample by variant calling


Competences:

  • Critically evaluate results of sequencing experiments from different perspectives (molecular biology, bioinformatics, genetics)
  • Independently analyze and interpret whole-genome DNA sequencing data and RNA-sequencing data

Lectures, theoretical and practical exercises, colloquia.

See Absalon

There is a significant academic overlap with NBIK15013U Genome Sequence Analysis, and it is therfore not recommended for students to attend both courses.

Written
Oral
Individual
Collective
Continuous feedback during the course of the semester
Peer feedback (Students give each other feedback)
ECTS
7,5 ECTS
Type of assessment
Continuous assessment
Type of assessment details
Participation in group work and colloquia.
The course uses continuous assessment with five different assignments. Students will work on each assignment in groups and present their results in written or oral form in group or individually, depending on the assignment.

The assignments/oral presentations are weighted with the following percentages: 10%, 30%, 15%, 30%, 15%, for assignments 1, 2, 3, 4, 5, respectively.

To pass the course, individual assignments need to be passed, with a total aggregated weight of at least 80%.
Aid
All aids allowed
Marking scale
passed/not passed
Censorship form
No external censorship
One internal examiner
Re-exam

Renewed hand-in of mandatory assignments/oral presentations.

Criteria for exam assessment

See Learning Outcome. 

  • Category
  • Hours
  • Lectures
  • 25
  • Preparation
  • 141
  • Practical exercises
  • 35
  • Exam
  • 5
  • English
  • 206

Kursusinformation

Language
English
Course number
NBIB25001U
ECTS
7,5 ECTS
Programme level
Bachelor
Duration

1 block

Placement
Block 2
Schedulegroup
B
Capacity
No limitation – unless you register in the late-registration period (BSc and MSc) or as a credit or single subject student.
Studyboard
Study Board for the Biological Area
Contracting department
  • Department of Biology
Contracting faculty
  • Faculty of Science
Course Coordinator
  • Robin Andersson   (5-7471646b7042646b71306d7730666d)
Saved on the 24-02-2025

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