
Genetics Course
Master genetics from foundational Mendelian principles to cutting-edge CRISPR genome editing and population genomics. This course gives you a rigorous, end-to-end understanding of how genetic information is stored, expressed, regulated, and applied. Whether you're pursuing research, medicine, or biotechnology, you'll build the analytical skills that modern genetics demands.
What you will learn:
You will learn how DNA is structured, replicated, and repaired, and how genes are transcribed and translated into functional proteins. You will explore chromosomal behaviour during mitosis and meiosis, and connect errors in cell division to real genetic disorders. The course covers gene regulation, epigenetics, and non-coding RNAs that control when and how genes are expressed. You will analyse genetic variation within populations and apply Hardy-Weinberg models to understand evolutionary forces. Genomics modules introduce sequencing technologies, genome assembly, and bioinformatics analysis pipelines. Applied genetics sections cover recombinant DNA techniques, CRISPR editing, genetic diagnostics, and the ethical implications of genomic data use.
How you study in practice Genetics Course
How you practise Genetics Course
For businesses looking to train their team
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 • 38 LessonsDuration between 4 and 360 hours (you decide)
Chapter 1HideHide detailsSee detailsFoundations of Genetics and Heredity
Foundations of Genetics and Heredity
Lesson 1 • Genotype, Phenotype, and Probability
Distinguishes genetic makeup from observable traits and applies probability to predict offspring ratios. Builds quantitative reasoning essential for genetics problem-solving.
Lesson 2 • DNA Structure and Composition
Covers the double-helix model, nucleotide components, and base-pairing rules. Provides the molecular foundation for all subsequent genetic concepts.
Lesson 3 • Mendelian Principles of Inheritance
Teaches Mendel's laws of segregation and independent assortment through pea-plant experiments. Grounds students in the rules that predict trait transmission.
Lesson 4 • The Cell as Genetic Unit
Introduces the cell's role as the structural basis of heredity. Connects cellular organisation to how genetic material is stored and transmitted.
Chapter 2HideHide detailsSee detailsChromosomes and Cell Division
Chromosomes and Cell Division
Lesson 1 • Mitosis and Somatic Cell Division
Details each phase of mitosis and cytokinesis in somatic cells. Connects accurate chromosome segregation to genetic stability across cell generations.
Lesson 2 • Chromosome Organisation and Karyotyping
Describes chromosome number, morphology, and karyotype construction. Establishes the physical basis for understanding division and inheritance patterns.
Lesson 3 • Meiosis and Gamete Formation
Contrasts meiosis I and II with mitosis, emphasising crossing over and haploid gamete production. Links meiotic events to genetic variation in offspring.
Lesson 4 • Chromosomal Abnormalities and Consequences
Covers nondisjunction, deletions, duplications, inversions, and translocations. Prepares students to connect chromosomal errors to clinical and developmental outcomes.
Chapter 3HideHide detailsSee detailsDNA Replication and Repair
DNA Replication and Repair
Lesson 1 • DNA Repair Pathways
Surveys base excision, nucleotide excision, mismatch, and double-strand break repair. Links pathway choice to lesion type and cell-cycle stage.
Lesson 2 • Proofreading and Fidelity Mechanisms
Explains how DNA polymerase proofreads and corrects errors during synthesis. Connects fidelity mechanisms to the low mutation rate observed in healthy cells.
Lesson 3 • Mutations and Their Consequences
Classifies point mutations, frameshifts, and large-scale alterations and their phenotypic effects. Bridges repair failure to heritable change and disease risk.
Lesson 4 • Mechanisms of DNA Replication
Covers the semi-conservative model, origin firing, and the roles of key replication enzymes. Establishes how the genome is accurately duplicated before each division.
Lesson 5 • DNA Damage Sources and Types
Catalogues endogenous and exogenous sources of DNA damage and the lesion types they produce. Provides context for understanding why multiple repair pathways exist.
Chapter 4HideHide detailsSee detailsGene Expression: Transcription and Translation
Gene Expression: Transcription and Translation
Lesson 1 • Translation and Ribosome Function
Details ribosome structure, initiation, elongation, and termination of translation. Links ribosomal mechanics to the fidelity of protein synthesis.
Lesson 2 • Transcription in Prokaryotes and Eukaryotes
Compares bacterial and eukaryotic transcription machinery, promoters, and termination signals. Highlights structural differences that affect gene regulation strategies.
Lesson 3 • Post-Translational Modifications
Surveys cleavage, folding, glycosylation, phosphorylation, and ubiquitination of proteins. Shows how modifications expand functional diversity beyond the primary sequence.
Lesson 4 • The Genetic Code and tRNA
Decodes the triplet codon system and explains tRNA structure and aminoacylation. Connects codon-anticodon pairing to accurate amino acid incorporation.
Lesson 5 • RNA Processing in Eukaryotes
Covers 5' capping, 3' polyadenylation, and splicing of pre-mRNA into mature mRNA. Explains how processing expands protein diversity from a limited gene set.
Chapter 5HideHide detailsSee detailsGene Regulation and Epigenetics
Gene Regulation and Epigenetics
Lesson 1 • DNA Methylation and Epigenetic Memory
Describes CpG methylation patterns, maintenance methyltransferases, and their role in stable gene silencing. Explains how epigenetic marks are propagated through cell division.
Lesson 2 • Non-Coding RNAs in Gene Regulation
Surveys miRNA, siRNA, lncRNA, and piRNA roles in post-transcriptional and transcriptional silencing. Highlights their importance in development and disease.
Lesson 3 • Chromatin Remodelling and Histone Modification
Explains how histone acetylation, methylation, and chromatin remodelling complexes alter DNA accessibility. Links chromatin state to transcriptional activation or silencing.
Lesson 4 • Prokaryotic Transcriptional Regulation
Uses the lac and trp operons to illustrate negative and positive control of gene expression. Establishes regulatory logic that underpins more complex eukaryotic systems.
Lesson 5 • Eukaryotic Transcriptional Control
Covers enhancers, silencers, transcription factors, and mediator complexes in eukaryotes. Connects combinatorial factor binding to tissue-specific and developmental gene expression.
Chapter 6HideHide detailsSee detailsGenetic Variation and Population Genetics
Genetic Variation and Population Genetics
Lesson 1 • Sources of Genetic Variation
Identifies mutation, recombination, and gene flow as primary generators of allelic diversity. Connects variation sources to the raw material for natural selection.
Lesson 2 • Molecular Markers and Population Studies
Surveys SNPs, microsatellites, and structural variants used to measure population diversity. Connects marker data to phylogenetic and ancestry inference.
Lesson 3 • Hardy-Weinberg Equilibrium
Derives and applies the Hardy-Weinberg principle to calculate expected genotype frequencies. Serves as the null model for detecting evolutionary change in populations.
Lesson 4 • Evolutionary Forces Altering Allele Frequencies
Analyses natural selection, genetic drift, mutation pressure, and gene flow as forces that shift allele frequencies. Distinguishes adaptive from neutral evolutionary change.
Lesson 5 • Linkage Disequilibrium and Haplotypes
Explains non-random allele associations across loci and how recombination erodes linkage disequilibrium over time. Prepares students for genome-wide association study interpretation.
Chapter 7HideHide detailsSee detailsGenomics and Sequencing Technologies
Genomics and Sequencing Technologies
Lesson 1 • Long-Read and Single-Cell Sequencing
Introduces nanopore and single-molecule real-time sequencing alongside single-cell RNA-seq. Highlights how these technologies resolve structural variants and cell-type heterogeneity.
Lesson 2 • Comparative and Functional Genomics
Uses synteny, ortholog identification, and genome-wide association studies to link sequence to function. Connects comparative analysis to understanding gene conservation and disease.
Lesson 3 • Sanger Sequencing and Early Genomics
Explains chain-termination sequencing chemistry and its role in early genome projects. Provides historical context for appreciating next-generation advances.
Lesson 4 • Next-Generation Sequencing Platforms
Covers sequencing-by-synthesis, library preparation, and cluster amplification in short-read platforms. Connects throughput and cost advantages to broad research applications.
Lesson 5 • Genome Assembly and Annotation
Describes de novo assembly algorithms, reference-guided mapping, and gene annotation pipelines. Prepares students to evaluate genome assembly quality metrics.
Chapter 8HideHide detailsSee detailsGenetic Engineering and Applied Genetics
Genetic Engineering and Applied Genetics
Lesson 1 • Genetic Testing and Diagnostics
Covers carrier screening, prenatal diagnosis, pharmacogenomics, and direct-to-consumer testing. Connects molecular tools to clinical decision-making and personalised medicine.
Lesson 2 • Polymerase Chain Reaction and Variants
Explains PCR primer design, thermocycling, and quantitative and digital PCR variants. Connects amplification techniques to diagnostics, cloning, and expression analysis.
Lesson 3 • CRISPR-Cas9 Genome Editing
Details guide RNA design, Cas9 cutting, and HDR vs. NHEJ repair outcomes. Positions CRISPR as the dominant tool for precise genome modification across organisms.
Lesson 4 • Recombinant DNA Technology
Covers restriction enzymes, ligation, vector design, and cloning strategies. Establishes the foundational toolkit for inserting and expressing foreign genes.
Lesson 5 • Transgenic Organisms and Gene Therapy
Surveys methods for generating transgenic plants, animals, and viral gene delivery for therapeutic use. Evaluates efficacy, off-target risks, and regulatory considerations.
Your valid completion certificate
This course is for you:
Biology undergraduates: building a rigorous foundation before advanced coursework.
Pre-med students: connecting molecular mechanisms to clinical and diagnostic contexts.
Biotech professionals: expanding lab skills into genomics and genome-editing territory.
Science teachers: refreshing and deepening genetics content for classroom delivery.
Curious science enthusiasts: exploring heredity and genomics beyond popular-science coverage.
Career changers: entering life sciences from adjacent fields like chemistry or data science.
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