Monique
Staff Emeritus
Science Advisor
Gold Member
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The way it works is that there are defined places on the genome that are highly variable. An example are VNTRs (variable number of tandem repeats) for instance [CATG]n. The code CATG is repeated n times, where n is highly polymorphic eg. it is unlikely that two people have the same lenght.
You can determine the length of that particular VNTR in a individual, at the same time you determine the length of a number of other VNTRs.
An example of the results from a SINGLE VNTR are given here
http://www.people.virginia.edu/~rjh9u/gif/vntr1.gif
You see a pedigree with two parents and four children below, you can see how many patterns are possible within just that one family.
You can determine the length of that particular VNTR in a individual, at the same time you determine the length of a number of other VNTRs.
An example of the results from a SINGLE VNTR are given here
http://www.people.virginia.edu/~rjh9u/gif/vntr1.gif
You see a pedigree with two parents and four children below, you can see how many patterns are possible within just that one family.
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