Genetic Mapping is the process of determining the location and order of genes or genetic markers on chromosomes. It provides insights into inheritance patterns, identifies disease-associated genes, and facilitates molecular genetics research. There are several types of genetic maps: linkage maps, based on recombination frequencies where closely linked genes are inherited together; physical maps, which measure actual distances in base pairs between genes or markers; and comparative maps, which compare genomes across species to identify conserved regions. Methods of genetic mapping include pedigree analysis, which studies inheritance in families; recombination analysis, estimating gene distances via crossover events; and the use of molecular markers such as microsatellites, SNPs, and RFLPs for high-resolution mapping. Modern approaches like genome-wide association studies (GWAS) allow identification of genes linked to traits or diseases across large populations. Applications of genetic mapping include locating disease-causing genes, assisting in marker-based therapies, understanding human evolution and population genetics, and identifying candidate genes for functional studies. Overall, genetic mapping is a foundational tool in human genetics, critical for research, diagnostics, and advancing personalized medicine.
- Linkage Analysis
- DNA Recombination
- Genetic Markers