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Chunk #22 — Methods — Genotyping, Quality Control, and Imputation

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Identification of 15 genetic loci associated with risk of major depression in individuals of European descent.
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DNA extraction and genotyping were performed on saliva samples by National Genetics Institute (NGI), a CLIA licensed clinical laboratory and a subsidiary of Laboratory Corporation of America. Samples were genotyped on one of four genotyping platforms. The V1 and V2 platforms were variants of the Illumina HumanHap550+ BeadChip, including about 25,000 custom SNPs selected by 23andMe. The V3 platform was based on the Illumina OmniExpress+ BeadChip, with custom content to improve the overlap with theV2 array. The V4 platform use most recently is a fully custom array, including a lower redundancy subset of V2 and V3 SNPs with additional coverage of lower-frequency coding variation. The platforms contained 586,916; 584,942; 1,008,948; and 570,000 SNPs, respectively. Samples that failed to reach 98.5% call rate were re-analyzed. Individuals whose analyses failed repeatedly were re-contacted by 23andMe customer service to provide additional samples, as is done for all 23andMe customers.