
Statistical Genomics Course
Master the statistical methods powering modern human genetics research. This course takes you from population genetics fundamentals through GWAS, polygenic scores, and causal inference — equipping you with the analytical toolkit to extract meaningful biological insights from large-scale genomic datasets.
What you will learn:
Apply probability models and multiple-testing corrections to genome-wide genomic analyses.
Process, quality-control, and prepare sequencing data using industry-standard file formats and pipelines.
Quantify linkage disequilibrium, perform genotype imputation, and reconstruct haplotype structure.
Design and execute GWAS, interpret Manhattan plots, and adjust for population stratification.
Construct and evaluate polygenic scores for disease risk prediction across ancestries.
Integrate eQTL mapping, fine-mapping algorithms, and functional annotations to identify causal variants.
How you study in practice Statistical Genomics Course
How you practice Statistical Genomics Course
For companies looking to train their teams
With Dedika for businesses, the course includes exercises and examples tailored to your own business and the way your company needs.
Course Content
8 Chapters • 37 LessonsDuration between 4 and 360 hours (you decide)
Chapter 1HideHide detailsSee detailsFoundations of Genetics and Genomics
Foundations of Genetics and Genomics
Lesson 1 • Genome Structure and Organization
Covers chromosomes, genes, regulatory elements, and genome architecture. Establishes biological vocabulary needed throughout the course.
Lesson 2 • DNA Variation and Mutation Types
Introduces SNPs, indels, CNVs, and structural variants. Connects variant classes to downstream statistical modeling choices.
Lesson 3 • Population Genetics Fundamentals
Introduces allele frequencies, Hardy-Weinberg equilibrium, and evolutionary forces. Grounds statistical models in population-level thinking.
Lesson 4 • Gene Expression and Regulation
Explains transcription, translation, and epigenetic control. Provides context for expression-based genomic analyses covered later.
Chapter 2HideHide detailsSee detailsProbability and Statistics for Genomics
Probability and Statistics for Genomics
Lesson 1 • Hypothesis Testing in Genomics
Covers null hypothesis testing, p-values, and power analysis. Prepares students for the multiple-testing challenges unique to genomics.
Lesson 2 • Probability Theory Essentials
Covers probability axioms, conditional probability, and Bayes' theorem. Provides the mathematical foundation for genomic inference.
Lesson 3 • Statistical Inference and Estimation
Teaches maximum likelihood estimation and confidence intervals. Connects estimation theory to parameter inference in genomic models.
Lesson 4 • Key Probability Distributions
Introduces binomial, Poisson, normal, and beta distributions. Links each distribution to specific genomic data-generating processes.
Lesson 5 • Multiple Testing Correction
Addresses Bonferroni, FDR, and q-value methods for genome-wide tests. Directly enables valid inference across millions of genomic loci.
Chapter 3HideHide detailsSee detailsGenomic Data Formats and Quality Control
Genomic Data Formats and Quality Control
Lesson 1 • Sequencing Technologies Overview
Surveys short-read, long-read, and single-cell sequencing platforms. Connects platform characteristics to data quality and analysis strategy.
Lesson 2 • Standard Genomic File Formats
Introduces FASTQ, BAM, VCF, BED, and related formats. Enables students to navigate and manipulate genomic data pipelines.
Lesson 3 • Sample and Variant Quality Control
Teaches missingness, heterozygosity, relatedness, and batch-effect checks. Prevents confounded results in all subsequent analyses.
Lesson 4 • Read Alignment and Preprocessing
Covers reference genome alignment, duplicate marking, and base quality recalibration. Produces analysis-ready files for downstream statistics.
Lesson 5 • Genotype Calling and Variant Filtering
Explains variant calling algorithms and hard-filter strategies. Ensures high-quality variant sets for association and population analyses.
Chapter 4HideHide detailsSee detailsLinkage Disequilibrium and Haplotype Analysis
Linkage Disequilibrium and Haplotype Analysis
Lesson 1 • Linkage Disequilibrium Concepts
Defines LD, recombination, and allelic association between loci. Establishes why LD is central to GWAS and imputation strategies.
Lesson 2 • Statistical Phasing Methods
Introduces hidden Markov models and population-based phasing algorithms. Enables accurate haplotype reconstruction from unphased genotype data.
Lesson 3 • Haplotype Structure and Blocks
Covers haplotype block detection and tag SNP selection. Connects haplotype structure to efficient genotyping array design.
Lesson 4 • Genotype Imputation
Explains imputation using reference panels to infer untyped variants. Extends association study power beyond directly genotyped markers.
Chapter 5HideHide detailsSee detailsPopulation Structure and Ancestry
Population Structure and Ancestry
Lesson 1 • Principal Component Analysis in Genomics
Applies PCA to genotype matrices to capture ancestry axes. Provides the primary tool for visualizing and correcting population stratification.
Lesson 2 • Fixation Index and Population Differentiation
Introduces FST and related statistics for measuring between-population divergence. Connects differentiation metrics to selection and demographic inference.
Lesson 3 • Demographic History Inference
Covers coalescent theory and methods for inferring population size changes. Provides historical context for interpreting modern genomic variation.
Lesson 4 • Model-Based Ancestry Estimation
Covers admixture models and likelihood-based ancestry inference. Enables quantitative ancestry proportion estimation for diverse cohorts.
Chapter 6HideHide detailsSee detailsGenome-Wide Association Studies
Genome-Wide Association Studies
Lesson 1 • Replication and Meta-Analysis
Teaches replication strategies and fixed- and random-effects meta-analysis. Enables combining evidence across cohorts for robust discovery.
Lesson 2 • Confounding and Covariate Adjustment
Addresses population stratification, cryptic relatedness, and batch effects. Teaches covariate inclusion and genomic control correction.
Lesson 3 • GWAS Study Design Principles
Covers case-control and quantitative trait designs, sample size, and power. Ensures statistically valid and reproducible study architecture.
Lesson 4 • GWAS Results Interpretation
Covers Manhattan plots, genome-wide significance thresholds, and locus zoom. Translates statistical signals into biologically meaningful findings.
Lesson 5 • Association Test Statistics
Introduces chi-square, logistic regression, and linear regression for GWAS. Connects test choice to trait type and covariate structure.
Chapter 7HideHide detailsSee detailsFunctional Annotation and Fine-Mapping
Functional Annotation and Fine-Mapping
Lesson 1 • Expression Quantitative Trait Loci
Covers cis- and trans-eQTL mapping and tissue-specific expression effects. Links GWAS loci to gene regulation as a functional mechanism.
Lesson 2 • Pathway and Gene Set Enrichment
Applies enrichment tests to GWAS hits for biological pathway discovery. Connects statistical signals to mechanistic biological processes.
Lesson 3 • Statistical Fine-Mapping Methods
Introduces credible set construction and Bayesian fine-mapping algorithms. Narrows association signals to the most probable causal variants.
Lesson 4 • Genomic Annotation Resources
Surveys regulatory databases, conservation scores, and chromatin accessibility data. Provides the annotation toolkit for variant prioritization.
Lesson 5 • Colocalization Analysis
Teaches probabilistic colocalization of GWAS and eQTL signals. Identifies shared causal variants between trait association and gene expression.
Chapter 8HideHide detailsSee detailsPolygenic Scores and Complex Trait Prediction
Polygenic Scores and Complex Trait Prediction
Lesson 1 • Transferability Across Populations
Addresses PGS performance decay in non-discovery populations. Motivates diverse training data and ancestry-aware scoring strategies.
Lesson 2 • PGS Construction Methods
Covers P+T thresholding, LDpred, and penalized regression approaches. Enables students to select and implement appropriate scoring methods.
Lesson 3 • PGS Validation and Performance Metrics
Teaches R-squared, AUC, and calibration for score evaluation. Ensures rigorous assessment of predictive accuracy in target samples.
Lesson 4 • Clinical and Research Applications of PGS
Explores risk stratification, drug target prioritization, and phenome-wide studies. Connects PGS methodology to real-world genomic medicine use cases.
Lesson 5 • Polygenic Score Theory
Explains the additive genetic model and SNP heritability underlying PGS. Grounds score construction in quantitative genetic theory.
Your valid completion certificate
This course is for you:
Wet-lab biologist: ready to lead their own computational genomics analyses independently.
Epidemiology graduate student: needs statistical genetics depth beyond standard coursework offerings.
Clinical researcher: wants to interpret polygenic risk scores appearing in medical literature.
Bioinformatics professional: filling gaps in population genetics and association study methodology.
Data scientist: pivoting into human genomics from a general machine learning background.
Genetic counselor: seeking deeper quantitative literacy to engage with research findings critically.
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