meffil.qc.parameters | R Documentation |
Specify parameters for QC
meffil.qc.parameters(
colour.code = NULL,
control.categories = NULL,
sex.outlier.sd = 3,
meth.unmeth.outlier.sd = 3,
control.means.outlier.sd = 5,
detectionp.samples.threshold = 0.2,
beadnum.samples.threshold = 0.2,
detectionp.cpgs.threshold = 0.2,
beadnum.cpgs.threshold = 0.2,
snp.concordance.threshold = 0.9,
sample.genotype.concordance.threshold = 0.9
)
colour.code |
Default value = NULL |
control.categories |
Default value = control.probe.categories() |
sex.outlier.sd |
Sets the standard deviation multiple at which sex outliers are identified. Default value = 3. |
meth.unmeth.outlier.sd |
Sets the standard deviation multiple at which methylated/unmethylated signal outliers are identified. Default value = 3. |
control.means.outlier.sd |
Sets the standard deviation multiple at which control probe signals are identified as outliers. Default value = 5 |
detectionp.samples.threshold |
Maximum threshold on the fraction of undetected probes (probe detection is defined by setting the maximum probe detection p-value threshold parameter |
beadnum.samples.threshold |
Maximum threshold on the fraction of probes with too few detected beads (minimum number of detected beads is defined by setting the |
detectionp.cpgs.threshold |
Same as |
beadnum.cpgs.threshold |
Same as |
snp.concordance.threshold |
Minimum required concordance between supplied genotypes and genotypes estimated from a SNP probe. Default value = 0.99 |
sample.genotype.concordance.threshold |
Minimum required concordance between supplied genotypes and genotypes estimated from SNP probes for a given individual. Default value = 0.9 |
List of parameter values
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