By a GenomeWeb staff reporter

NEW YORK (GenomeWeb News) – The genetic risk for common, complex disease likely lies in many common SNPs combined with a few rare causal variants, according to a Nature Genetics study by an international team that developed a new statistical strategy for delving into the genetic architecture of such diseases.

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May
28
Sponsored by
PerkinElmer

This online seminar will demonstrate how RNA-seq analysis in a model organism can provide insights into human disease.