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slides in pdf format - Department of Statistics - Rice University

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Us<strong>in</strong>g Population Structure to Map Complex Diseases<br />

We have developed an algorithm to map complex diseases. We do not explicitly<br />

identify subpopulations. Instead, we construct a neighborhood <strong>of</strong> families for each<br />

family by putt<strong>in</strong>g weights on families accord<strong>in</strong>g to family relatedness measures.<br />

• Estimate family relatedness us<strong>in</strong>g marker data. The family relatedness<br />

measures are the averaged relatedness coef between all <strong>in</strong>ter-family <strong>of</strong>fspr<strong>in</strong>g<br />

comb<strong>in</strong>ations, which can be estimated by, for example, Queller’s Method [ Queller<br />

1989, Lynch et al 1999 ]<br />

ˆr xy =<br />

1<br />

2 (δ ac + δ ad + δ bc + δ bd ) − p a − p b<br />

1 + δ ab − p a − p b<br />

where (a, b), (c, d) are genotypes <strong>of</strong> <strong>in</strong>dividual x and y. p a is the population<br />

frequency <strong>of</strong> allele a.<br />

• Def<strong>in</strong>e a weight<strong>in</strong>g system that falls <strong>of</strong>f with <strong>in</strong>creas<strong>in</strong>g distance away along<br />

the chromosome and also with decreas<strong>in</strong>g relatedness across families.<br />

Keck Fellows Meet<strong>in</strong>g, July 2004 10

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