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The goal of the IIPGA is to discover and model the associations between nucleotide sequence
variations, primarily Single Nucleotide Polymorphisms (SNPs) and Insertion/Deletion polymorphisms
(Indels), in the genes of the innate immunity pathway in humans. The Program is two-fold:
Part 1 identifies
the common variable sites through sequencing and establishes their relative allele
frequencies and haplotypes in four human populations having different evolutionary histories.
Part two utilizes this data in case-control association studies of airways disease (i.e., asthma and
chronic obstructive pulmonary disease). We have available to us a full array of bioinformatics tools
for performing association analysis in human genetics. These tools and resources are important for
any association study relating innate immune responses to disease in a whole host of complex common
human disorders such as: airways disease, myocardial infarction, hypertension, stroke, Crohn's Disease,
allergy, and diabetes to name a few.
Two of the major goals of the IIPGA are to establish a website to disseminate
data to the public and develop an
educational training program that
will allow individuals with varying levels of knowledge
and experience to become acquainted with modern genetic techniques.
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