Course Overview:

This in-depth course covers the foundational principles of genetics, the intricacies of DNA, human genome analysis, and the mechanisms behind genetic disorders and diseases. Ideal for students and professionals in life sciences, this course provides a structured approach to understanding genetic mutations, DNA repair, sequencing techniques, and the genetic basis of diseases like Huntington's, Down Syndrome, and Parkinson’s.

Section 1: Introduction to Genetics

Begin your journey into the world of genetics with a comprehensive introduction. Learn about the fundamentals of genetics, exploring its core principles and foundational concepts over three engaging lectures.

Section 2: Cells, Proteins, Chromosomes, and Gene Mutations

Dive into the structural and functional aspects of genetics by understanding the roles of cells, proteins, and chromosomes. This section highlights the causes and effects of gene mutations through a detailed, step-by-step analysis.

Section 3: Human Genome and DNA

Explore the structure and significance of the human genome. Gain insights into DNA’s role as the genetic material, and understand its replication, coding, and regulation processes. This section establishes a solid foundation for studying advanced genetic concepts.

Section 4: Important Concepts in Genetics

This section breaks down critical genetic concepts into five detailed lectures. Topics include gene regulation, inheritance patterns, and the molecular basis of phenotypes, providing a comprehensive understanding of how genetics influences life.

Section 5: Mutagenesis and DNA Repair

Discover the mechanisms of mutagenesis—the processes by which genetic mutations occur—and the body's natural DNA repair mechanisms. Learn about DNA-protein interactions and their critical role in maintaining genetic integrity.

Section 6: Sequencing and Analysis

Uncover the techniques used in genetic sequencing and data analysis. From Sanger sequencing to next-generation techniques, this section offers a step-by-step guide to interpreting genetic data and its applications in research and medicine.

Section 7: Genetic Disorders

Learn about the genetic basis of disorders, their inheritance patterns, and modern diagnostic techniques. This section explores genetic testing methods and dives into specific conditions, helping learners understand how and why these disorders arise.

Section 8: Understanding Diseases

Study a range of genetic diseases, including:

• Huntington's Disease: A neurodegenerative condition caused by genetic mutation.

• Sickle Cell Disease: A disorder affecting red blood cells.

• Down Syndrome: A chromosomal condition leading to developmental delays.

• Parkinson's Disease: A progressive nervous system disorder.

• Thalassemia, Cerebral Palsy, and Bipolar Disorder: Conditions with varied genetic underpinnings.

• Gaucher's Disease: A rare genetic disorder impacting metabolism.

This section provides real-world examples of how genetics influences health and offers insights into diagnosis and management.