Chunk #18 — Results — Application to GWAS

Source

Annotation of functional variation in personal genomes using RegulomeDB.

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yes

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Classifying variants based on the above criteria is also highly informative to genome-wide association studies. We demonstrate this by repeating the search for a causative SNV for systemic lupus erythematosus in a 500-KB region around the TNFAIP3 gene (Adrianto et al. 2011).