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Each column represents
* CHROM : Chromosome Name
* BEGIN, END : Base position of the variant on each side
* MARKER_ID : [CHROM]:[POS]_[REF]/[ALT]_[ANNOTATION] formatted marker ID. [ANNOTATION] information will be available only with --anno option
* NS : Number of samples with non-missing genotypes
* AC : Non-reference allele count
* CALLRATE : Genotype call rate
* MAF : Minor allele frequency
* PVALUE : P-value
The rest of columns varies by statistical tests. For example, in b.score test, SCORE represents score test statistics, N.CASE and N.CTRL represents the case/control counts, and AF.CASE and AF.CTRL represents the case/control allele frequencies.
