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Gene Mapping Video Lecture - NEET

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1. What is gene mapping?
Gene mapping is the process of determining the precise location of a gene on a chromosome. It involves identifying the position of genes and their relative distances from each other on a chromosome.
2. How is gene mapping done?
Gene mapping can be accomplished through various techniques, such as linkage analysis and physical mapping. Linkage analysis examines how genes are inherited together, while physical mapping uses techniques like DNA sequencing to directly locate genes on a chromosome.
3. What is the significance of gene mapping?
Gene mapping plays a crucial role in understanding the genetic basis of various diseases and traits. It helps identify genes associated with specific conditions, enabling researchers to study their functions and develop targeted treatments or interventions.
4. Can gene mapping help in predicting the risk of genetic diseases?
Yes, gene mapping can contribute to predicting the risk of genetic diseases. By identifying specific genes associated with certain disorders, geneticists can assess an individual's genetic profile and determine their likelihood of developing a particular condition.
5. Are there any limitations to gene mapping?
While gene mapping is a powerful tool, it does have limitations. It may not always provide a complete understanding of the complex interactions between genes and environmental factors that contribute to disease development. Additionally, gene mapping requires a large sample size and extensive data analysis, which can be time-consuming and costly.
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