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
21. Population Genetics
Allelic Frequency Changes
1:56 minutes
Problem 34c
Textbook Question
Textbook QuestionEvaluate the following pedigree, and answer the questions below. Which individual(s) in this family is/are inbred?
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Pedigree Analysis
Pedigree analysis is a method used to study the inheritance patterns of traits in families. It involves creating a diagram that represents family relationships and the transmission of genetic traits across generations. By analyzing the pedigree, one can identify carriers of specific traits, determine the likelihood of traits appearing in offspring, and assess the potential for genetic disorders.
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Pedigree Flowchart
Inbreeding
Inbreeding refers to the mating of individuals who are closely related genetically, which can increase the probability of offspring inheriting genetic disorders. In a pedigree, inbreeding is often indicated by a double line connecting two individuals, signifying a consanguineous relationship. Understanding inbreeding is crucial for evaluating genetic health and diversity within a family or population.
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Non-Random Mating
Genetic Disorders
Genetic disorders are diseases or conditions caused by abnormalities in an individual's DNA. These can be inherited from parents or arise from mutations. In the context of pedigree analysis, identifying individuals who may carry genetic disorders is essential, especially in inbred populations, where the risk of recessive disorders increases due to a higher likelihood of inheriting the same alleles from both parents.
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Descriptive Genetics
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