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Chunk #15 — Results

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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.
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The ADHD cohort comprised of 335 complete parent–child trios of European descent recruited from pediatric and behavioral clinics that passed genotype and CNV analysis quality metrics (see Methods). A set of 2026 ethnically matched, disease-free children was used as a healthy control group. All samples were genotyped using the Illumina HumanHap550K BeadChip and a single consistent protocol. Genotype data were uniformly analyzed for CNVs using Illumina's BeadStudio software in combination with a customized adaptation of the circular binary segmentation algorithm.29