2773 Chromosome Mapping Terms and Definitions at www.MedicalGlossary.org

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Chromosome Mapping

Definition: Any method used for determining the location of and relative distances between genes on a chromosome.
Also Called: Genome Mapping

Chromosome Mapping Categories.
Chromosome Walking - A technique with which an unknown region of a chromosome can be explored. It is generally used to isolate a locus of interest for which no probe is available but that is known to be linked to a gene which has been identified and cloned. A fragment containing a known gene is selected and used as a probe to identify other overlapping fragments which contain the same gene. The nucleotide sequences of these fragments can then be characterized. This process continues for the length of the chromosome.
Physical Chromosome Mapping - Mapping of the linear order of genes on a chromosome with units indicating their distances by using methods other than genetic recombination. These methods include nucleotide sequencing, overlapping deletions in polytene chromosomes, and electron micrography of heteroduplex DNA. (From King & Stansfield, A Dictionary of Genetics, 5th ed)

Chromosome Mapping Definitions and Terms

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