Genomics, Systems Biology and Bioinformatics
Unified framework for multi-omics teaching
One framework, two pathways
- Reuse concepts and worked examples across both harmonized MSc outlines.
- Select depth and exercises to match each pathway’s learning objectives.
- Keep study design, computation and biological interpretation connected.
Use the teaching materials
- Read the module and identify the measurement and assumptions.
- Run the practical and predict the effect of one change.
- Attempt exercises before opening suggested answers.
- Explain what the result supports and what needs further evidence.
Course map · Modules · Practicals
B01 Biological questions
- Define the production trait, population and decision time.
- Separate intervention, association and prediction.
- Choose measurements that answer the question.
Discuss: Does a day14 profile qualify as a baseline predictor?
B02 Design and sampling
- Identify the independently allocated experimental unit.
- Cross treatment groups with processing batches.
- Record animal, specimen, tissue, time and handling.
Discuss: Can adjustment separate perfectly confounded treatment and batch?
B03 Databases and identifiers
- Distinguish study, sample, gene, transcript and protein records.
- Preserve species, assembly and annotation versions.
- Audit unmatched and one-to-many mappings.
Discuss: Does a duplicated annotation row create a new measurement?
B04 Reproducible data handling
- Define feature and sample dimensions.
- Align by stable identifiers; check uniqueness and missing matches.
- Preserve raw inputs and record transformations.
Discuss: Would equal dimensions detect a sample-order error?
B05 Genomic measurements
- Distinguish reads, assemblies, alignments and genotype calls.
- Specify quality encoding and the called-base denominator.
- Separate identity, homology and functional claims.
Discuss: Why can a high-identity short sequence be weak evidence?
B06 Transcriptomics
- Define biological replicates and the expression contrast.
- Separate exposure normalization, visualization and inference.
- Count-model variance and dispersion affect uncertainty.
Discuss: Do many reads replace independent animals?
B07 Epigenomics
- Record coverage, tissue and assay context.
- Distinguish within-cell changes from composition shifts.
- Regulatory association is not evidence of mediation by itself.
Discuss: Can bulk methylation change while each cell type stays constant?
B08 Proteomics
- Separate peptide identification, protein inference and abundance.
- Preserve the measurement scale and observation counts.
- Missing abundance is not a measured zero.
Discuss: What does a one-unit log2 difference represent?
B10 Microbiomics
- Define sampling site, time and profiling method.
- Relative read fractions do not measure total microbial load.
- Host associations can share diet, genotype and technical drivers.
Discuss: Can a fraction decrease while absolute amount stays constant?
B11 Phenomics
- Define phenotype units, time window and coverage.
- Repeated sensor rows remain nested within animals.
- Use only information available at the decision time.
Discuss: How many independent allocations are in a million sensor rows?
B12 Statistics and validation
- Distinguish conditional inference from prediction.
- Fit preprocessing and tuning within training data.
- Evaluate on independent units matching deployment.
Discuss: When does a test set become a tuning set?
B13 Association and regulation
- State counted alleles, covariates and relatedness assumptions.
- LD can make several candidates tag the same signal.
- GWAS, eQTL, TWAS and prediction answer different questions.
Discuss: Does a correlated eQTL and trait signal prove mediation?
B14 Pathways and networks
- Define the eligible background and selection null.
- State what an edge measures and how it is selected.
- Enrichment and correlation do not directly measure causal activity.
Discuss: How would changing the background alter enrichment?
B15 Multi-omics integration
- Match animal, tissue and time across layers.
- Choose an integration strategy and justified block weights.
- Evaluate missingness and shared biological/technical drivers.
Discuss: Are two correlated layers independent replications?
B16 Advanced methods
- Cell and spatial resolution do not create independent allocations.
- Keep specimens/animals separated for new-animal prediction.
- Evaluate measurement, model and mechanistic evidence separately.
Discuss: Can spatial proximity establish a molecular interaction?
B17 Research integrity
- Document provenance, exclusions and exploratory decisions.
- Share only data allowed by the governing agreements.
- Verify and disclose AI contributions appropriately.
Discuss: Does a checksum certify biological validity?
B18 Animal-production synthesis
- Connect each assay to the defined production question.
- Compare strategies on the same independent evaluation animals.
- Report uncertainty, alternatives and justified follow-up.
Discuss: Does a predictive improvement identify an intervention target?
Worked thread through the course
- Plan an animal-level diet study and matched assays.
- Verify sample identity and assay-specific quality.
- Analyse RNA counts and expression contrasts.
- Examine pathways and cross-layer relationships.
- Compare predictive strategies with training-only transformations.
- Write an interpretation or proposal at the level the evidence supports.
Complete the pathway
GSB: data resources → computation → association → networks → integration.
Multi-Omics: technologies → sampling/design → processing → integration → production applications.
Both use the same maintained module and practical sources. The map preserves original module numbering and assessment weights.