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Chunk #6 — SNP Analysis — Discovery genotyping and quality control

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Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
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(v) intensity failure: individuals were excluded if the mean of their A and B allele intensities from 10000 SNPs on chromosome 22 was outlying when compared to the sample at large. (vi) identity: prior to being genotyped, ~30 SNPs were typed using Sequenom® at the WTSI. If the concordance between the genome-wide & Sequenom® genotypes was <90% then the individual is excluded on the basis of unknown identity. (vii) ethnic outliers: cases with a distance to CEU > 30 based on a principal components analysis were excluded.