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Chunk #13 — Materials And Methods — SNP quality control

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A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
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As expected, we observed negative correlation between the proportion of ME per SNP and p-value for HWE. To minimize genotyping errors we excluded SNPs with p-value <10-6 for HWE and ME > 4%. Remaining erroneous genotypes were set as missing. PLINK software was used for quality control steps described above (Purcell et al. 2007).