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4<br />

Motivation: ”Omics” Data in Population-Based Studies<br />

• In genome-wide assocation studies, a million SNP markers are<br />

genotyped across the genome to study the association of<br />

common genetic variants and disease phenotypes (case/control<br />

status).<br />

• The massive whole genome-wide sequencing data are rapidly<br />

available, e.g., the 1000 genome project, to study the effects of<br />

rare variants.<br />

March, 2009<br />

Xihong Lin

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