The HumanLinkage V Panel Set is optimized to detect recombination events. Linkage analysis is a powerful approach for mapping the location of disease-causing loci. The likelihood of a recombination event occurring between two markers is related to the distance between them. Markers closest to a disease gene will co-segregate most strongly with the disease phenotype.
The panel's 6,056 SNP markers were chosen from highly validated HapMap DNA assays to optimize information content, enabling researchers to extract the greatest amount of data from the least number of markers. Every SNP marker has been robustly validated for physical and genetic map positions, distances, and unique sequence identification.
Catalog IDs: GT-17-240
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