LF:BLKG051x Clinical Genetics - practice - Course Information
BLKG051x Clinical Genetics - practice
Faculty of MedicineSpring 2009
- Extent and Intensity
- 0/0. 3 credit(s). Type of Completion: z (credit).
- Guaranteed by
- doc. MUDr. Milan Dastych, CSc., MBA
Department of Laboratory Methods – Departments of Non-medical Branches – Faculty of Medicine
Contact Person: Michaela Gregorovičová - Prerequisites (in Czech)
- BLKG0311 Clinical Genetics
- 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
- Laboratory Assistant (programme LF, B-SZ)
- Course objectives
- Specialist practice complements the practical part of education in Clinical Biochemistry, Clinical Hematology, Immunohematology and Transfusion medicine, Clinical Microbiology, Clinical Immunology, Clinical Genetics and Pathologic Anatomy – Histopathologic determination methods. Students become familiar with the organization of workflow processes and basic documentation of laboratory worksites and will perform select tasks and activities.
- Syllabus
- Peripheral blood taking for human cell cultivation, storage of symplex; Setting up of cell culture for assessment of congenital chromosomal aberrations; Setting up of cell culture for assessment of acquired chromosomal aberrations; Cell culture processing; Preparation of metaphase chromosomes for analysis of congenital and acquired chromosomal aberrations; Microscope and computer image analyses of metaphase chromosome; Result example s of interphase and metaphase Fluorescence in situ Hybridization (FISH); Examples of Spectral Karyotyping (SKY); Prenatal cytogenetic diagnostics – specificity; Peripheral blood taking for DNA analysis, DNA isolation methods; DNA quality control and determination of DNA concentration; RNA isolation; DNA amplification using PCR Metod; Detection of PCR products (agarose and polyacrylamide electrophoresis); Molecular genetic methods for detection of mutations in medical genetics (Denaturing Gradient Gel Electrophoresis - DGGE, Single-Strand Conformation Polymorphism - SSCP, Real-Time PCR, fragment analysis, sequencing) ;
- Literature
- FLODROVÁ, Eva, Alexandra ŽOURKOVÁ, Jan JUŘICA, Tomáš KAŠPÁREK and Renata GAILLYOVÁ. Molecular genetic analysis of CYP2D6 gene and used methods. In European Human Genetic Conference. 2008. URL URL info
- FLODROVÁ, Eva, Alexandra ŽOURKOVÁ, Jan JUŘICA and Renata GAILLYOVÁ. Molecular genetic identification of the major CYP2D6 alleles and utilization in psychiatric treatment. In 26th Collegium Internationale Neuro-Psychopharmacologicum Congress (CINP). 2008. ISSN 1461-1457. info
- VOJTÍŠKOVÁ, Marie, J. KADLECOVÁ, T. NOVOTNÝ, Renata GAILLYOVÁ, Hana KONEČNÁ, Jana KLÁNOVÁ and B. SEMRÁD. Molekulární diagnostika pacientů se syndromem prodlouženého QT intervalu (Molecular Diagnostics of Pacients with Long QT Syndromes). In Biochemie a molekulární biologie na prahu nového tisíciletí. 2000th ed. Brno: Masarykova univerzita, 2000, p. 83-84. ISBN 80-210-2266-3. info
- JIČÍNSKÁ, H., J. MAREK, Věra BRYŠOVÁ, Renata GAILLYOVÁ, Jiří LITZMAN, Petr KUGLÍK and Jiří NAVRÁTIL. Delece 22q11 chromozomu u vrozených srdečních vad (VSV) (Chromosome 22q11 deletion in congenital heart defects )CHD)). Česko-slovenská pediatrie. Praha: ČLS, 1998, vol. 53, suppl. 1, p. 67. ISSN 0069-2328. info
- Assessment methods
- credit
- Language of instruction
- Czech
- Enrolment Statistics (Spring 2009, recent)
- Permalink: https://is.muni.cz/course/med/spring2009/BLKG051x