PřF:C7175 DNA diagnostics - Course Information
C7175 DNA diagnostics
Faculty of ScienceSpring 2025
- Extent and Intensity
- 2/0/0. 4 credit(s). Recommended Type of Completion: zk (examination). Other types of completion: k (colloquium).
In-person direct teaching - Teacher(s)
- prof. RNDr. Omar Šerý, Ph.D. (lecturer)
- Guaranteed by
- prof. RNDr. Omar Šerý, Ph.D.
Department of Biochemistry – Chemistry Section – Faculty of Science
Supplier department: Department of Biochemistry – Chemistry Section – Faculty of Science - Prerequisites
- C6200 Biochemical Methods
Without preconditions. - Course Enrolment Limitations
- The course is also offered to the students of the fields other than those the course is directly associated with.
- fields of study / plans the course is directly associated with
- Applied Biochemistry (programme PřF, B-AB)
- Applied Biochemistry (programme PřF, B-CH)
- Biochemistry (programme PřF, M-CH)
- Biochemistry (programme PřF, N-BCH)
- Biochemistry (programme PřF, N-BCH3)
- Biochemistry (programme PřF, N-CH)
- Biology (programme PřF, N-BI)
- Course objectives
- At the end of the course students should be able to understand and explain practical use of DNA diagnostics in human medicine, veterinary medicine etc.
- Learning outcomes
- At the end of the course students will understand principles of PCR method, RealTime PCR, sequencing, next generation sequencing, restriction analysis, work with DNA databases, European Union legislation on in vitro medical devices, use of DNA diagnostics in medical practice. Students will have the theoretical knowledge of methods used in clinical laboratories for DNA diagnosis of bacterial and viral pathogens.
- Syllabus
- 1. General introduction, history of DNA diagnostics (discovery of DNA structure, discovery of PCR principle). 2. Principle of polymerase chain reaction - master mixes, template DNA, primers, buffer, dNTP, DNA polymerase, PCR steps, thermocycler, methods of multiplying DNA in vitro without using DNA polymerase. 3. Detection of amplified DNA, agarose gels, polyacrylamide gels, electrophoresis, PCR in situ, restriction analysis. 4. Real Time PCR, principle, sybrgreen, TaqMan, molecular beacons, detection of point polymorphisms, quantification by RealTime PCR, DNA isolation methods. 5. Principles and use of genotyping methods (RFLP methods, methods based on qPCR, SNaPshot method, chip technologies, CNV analysis). 6. Principles of NGS methods (library preparation, pyrosequencing, Illumina technology, Ion PGM system, nanoball sequencing). 7. Use of NGS methods in diagnostics (genome, exome, transcriptome, metagenome, resistome, targeted resequencing). 8. Modifications of PCR methods used in diagnostics, celiac disease diagnostics. 9. DNA diagnostics in medicine: legislative requirements for in vitro diagnostic medical devices (IVDR). 10. Medical virology: practical use of DNA diagnostics in direct virus detection. Detection of HIV, SARS-CoV-2, viral hepatitis, herpes viruses, papillomaviruses, etc. 11. Medical microbiology and parasitology: practical use of DNA diagnostics in direct detection of microorganisms. Detection of MTB, borrelia, chlamydia, mycoplasmas, ureaplasmas, etc.
- Literature
- recommended literature
- Manual of commercial methods in clinical microbiology. Edited by Allan L. Truant. Washington: ASM Press, 2002, xix, 481 s. ISBN 1-55581-189-2. info
- RAPLEY, Ralph. The nucleic acid protocols : handbook. Totowa, New Jersey: Humana Press, 1999, xxii, 1050. ISBN 0-89603-459-3. info
- Teaching methods
- Lectures with PowerPoint presentations and recommended books for self study.
- Assessment methods
- Oral exam
- Language of instruction
- Czech
- Further Comments
- The course is taught annually.
The course is taught: every week. - Listed among pre-requisites of other courses
- Enrolment Statistics (recent)
- Permalink: https://is.muni.cz/course/sci/spring2025/C7175