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Chunk #4 — Design of the COGA Study — Genetic Analysis

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Defining alcohol-related phenotypes in humans. The Collaborative Study on the Genetics of Alcoholism.
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Because the researchers did not know in advance which chromosomes would carry genetic factors influencing the development of alcoholism and related phenotypes, the genetic analyses involved a survey of all chromosomes—that is, the entire genome. To follow the inheritance of different regions of each chromosome, the researchers used more than 300 microsatellite markers—short, repeated DNA sequences that exist in many variants (i.e., alleles) and whose locations on the chromosomes are known. Every person carries two copies of each marker, one inherited from the mother and one inherited from the father. Because of their diversity, these two copies of each marker are likely to differ, allowing researchers to follow the inheritance of the corresponding chro mosomal regions in a family. Such a genomewide search strategy allows for the discovery of novel genes not previ ously considered candidates for influ encing alcoholism risk.