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Chunk #58 — METHODS — Overlap of common ADHD risk variants with rare protein-truncating variants (rPTVs).

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Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains.
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The burden of rPTVs and rare synonymous (rSYNs) in cases compared to controls was tested for the three gene sets with logistic regression corrected using the following covariates: birth year, sex, first ten principal components, number of rSYN, percentage of target with coverage > 20x, mean read depth at sites within the exome target passing VQSR, total number of variants, sequencing wave.