The course will introduce students to basic bioinformatics including best practice when setting up and managing bioinformatics projects. The course covers introduction to high throughput sequencing technologies and will give students hands-on experience with the analysis of data from various sequencing platforms.
This course is primarily aimed at PhD candidates admitted to the PhD Programme in Health Sciences but is also open to other applicants.
General terms for admission to the course is a completed master's degree in molecular biology or equivalent qualification (e.g. completed MABIO4400)
How to Apply
See application process information for PhD courses.
The application deadline is two months before the course starts.
Course period: cancelled autumn 2020
The course consists of three weeks consecutive work that includes the following teaching methods: self-study including exercises/questionnaires related to background theory (one week), lectures and seminars (one week), and practical exercises in the use of different software programmes for analysis of HTS data (one week). The outcomes of the practical exercises in last week are discussed in plenary sessions.
Applications that are included in the practical part are processing of raw data reads, control of quantity and quality of data (FASTQC), expression analysis of small RNA sequencing data (miRNA) and transcriptome sequencing/microarray (mRNA-seq, cDNA) data, and detection of variation (e.g. SNPs) after resequencing (variant calling).
All obligatory exercises must be completed to take the final exam. The final exam is a written examination with invigilation, 4 hours. One internal and one external examiner will assess the answer papers submitted by all candidates.
For more information about this course, take a look at the course description (student.oslomet.no).
There are no tuition fees for this course.
Questions about This Course?
You can contact us by e-mail if you have questions about this course.