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Bio Lab Research Paper Eportfolio
Bio Lab Research Paper Eportfolio
phenotypic effect sizes. Genome-wide association studies and wholegenome sequencing have allowed the ability for us to discover novel
genomic determinations of CVDs. GWAs and whole-genome
sequencings allows us to identify genes with previously unknown roles
in CVD.
The method they are using in the new update for GWAs is
analyzing single-nuclotide polymorphisms across the genome with a
case-control and continuous traits. They are also using exome and
genome sequencing which provides a strong research strategy for the
conditions that are pushed by uncommon variants.
They review the current state and knowledge we already have
obtained from CVDs which include coronary artery disease, stroke,
hypertension, and hypercholesterolemia. In this update they added
diabetes mellitus, inflammation, and pharmogenetics.