Introduction to Medical Genetics
Coverage is provided of the fundamental knowledge in human genetics and genetic systems of the mouse and other model organisms. Topics include: introduction to concepts of inheritance (DNA, chromatin, genes, chromosomes); the human genome (normal genetic variation, SNPs, comparative genomes, molecular mechanisms behind inheritance patterns, and mitochondrial genetics); mouse genetics (classical mouse genetics, genotype- and phenotype-driven approaches, QTL mapping); microarrays (expression, genomic, ChIP (chromatin IP on chip), bioinformatics and use of genome databases); genetic association studies (haplotype blocks, study design in complex disease and approaches to complex disease gene identification, pharmacogenetics and pharmacogenomics). Prerequisite: None. Credits: 2.
Topics
- introduction to concepts of inheritance (DNA
- chromatin
- genes
- chromosomes)
- the human genome (normal genetic variation
- SNPs
- comparative genomes
- molecular mechanisms behind inheritance patterns
- and mitochondrial genetics)
- mouse genetics (classical mouse genetics
- genotype- and phenotype-driven approaches
- QTL mapping)
- microarrays (expression
- genomic
- ChIP (chromatin IP on chip)
- bioinformatics and use of genome databases)
- genetic association studies (haplotype blocks
- study design in complex disease and approaches to complex disease gene identification
- pharmacogenetics and pharmacogenomics)
Topics explicitly listed in official catalogue description
Sources
- Course catalogue ↗2026-2027