Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
18. Molecular Genetic Tools
Methods for Analyzing DNA
1:30 minutes
Problem 10c
Textbook Question
Textbook QuestionDoes genetic analysis by ASO testing allow for detection of epigenetic changes that may contribute to a genetic disorder? Explain your answer.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
ASO Testing
Allele-Specific Oligonucleotide (ASO) testing is a molecular technique used to detect specific genetic mutations associated with diseases. It involves using short DNA sequences that are complementary to the target mutation, allowing for the identification of alleles in a sample. ASO testing is particularly useful for diagnosing single-gene disorders and can provide insights into the genetic basis of certain conditions.
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Epigenetics
Epigenetics refers to the study of heritable changes in gene expression that do not involve alterations to the underlying DNA sequence. These changes can be influenced by environmental factors and can affect how genes are turned on or off. Epigenetic modifications, such as DNA methylation and histone modification, can play a significant role in the development of genetic disorders, potentially impacting disease phenotypes.
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Genetic Disorders
Genetic disorders are diseases caused by abnormalities in an individual's DNA, which can result from mutations, chromosomal abnormalities, or epigenetic changes. These disorders can be inherited or arise de novo and can affect various bodily functions. Understanding the genetic and epigenetic factors involved in these disorders is crucial for diagnosis, treatment, and management strategies.
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