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Genetics Course
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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 are pursuing research, medicine, or biotechnology, you will build the analytical skills that modern genetics demands.

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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

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Course content

8 Chapters • 38 LessonsDuration between 4 and 360 hours (you decide)

Chapter 1See details

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 2See details

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 3See details

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 4See details

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 5See details

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 6See details

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 7See details

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 8See details

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.

Certification

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 educators: 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.

What our students say

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