Package 'WGCNA' - Laboratory Web Sites - UCLA
Package 'WGCNA' - Laboratory Web Sites - UCLA
Package 'WGCNA' - Laboratory Web Sites - UCLA
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16 blockwiseConsensusModules<br />
minCoreKME a number between 0 and 1. If a detected module does not have at least minModuleKMESize<br />
genes with eigengene connectivity at least minCoreKME, the module is disbanded<br />
(its genes are unlabeled and returned to the pool of genes waiting for<br />
mofule detection).<br />
minCoreKMESize<br />
see minCoreKME above.<br />
minKMEtoStay genes whose eigengene connectivity to their module eigengene is lower than<br />
minKMEtoStay are removed from the module.<br />
reassignThresholdPS<br />
per-set p-value ratio threshold for reassigning genes between modules. See Details.<br />
mergeCutHeight<br />
dendrogram cut height for module merging.<br />
impute logical: should imputation be used for module eigengene calculation See<br />
moduleEigengenes for more details.<br />
getTOMs<br />
deprecated, please use saveTOMs below.<br />
saveTOMs logical: should the consensus topological overlap matrices for each block be<br />
saved and returned<br />
saveTOMFileBase<br />
character string containing the file name base for files containing the consensus<br />
topological overlaps. The full file names have "block.1.RData", "block.2.RData"<br />
etc. appended. These files are standard R data files and can be loaded using the<br />
load function.<br />
getTOMScalingSamples<br />
logical: should samples used for TOM scaling be saved for future analysis This<br />
option is only available when sampleForScaling is TRUE.<br />
trapErrors<br />
logical: should errors in calculations be trapped<br />
checkPower logical: should basic sanity check be performed on the supplied power If you<br />
would like to experiment with unusual powers, set the argument to FALSE and<br />
proceed with caution.<br />
numericLabels<br />
logical: should the returned modules be labeled by colors (FALSE), or by numbers<br />
(TRUE)<br />
checkMissingData<br />
logical: should data be checked for excessive numbers of missing entries in<br />
genes and samples, and for genes with zero variance See details.<br />
Details<br />
verbose<br />
indent<br />
integer level of verbosity. Zero means silent, higher values make the output<br />
progressively more and more verbose.<br />
indentation for diagnostic messages. Zero means no indentation, each unit adds<br />
two spaces.<br />
The function starts by optionally filtering out samples that have too many missing entries and genes<br />
that have either too many missing entries or zero variance in at least one set. Genes that are filtered<br />
out are left unassigned by the module detection. Returned eigengenes will contain NA in entries<br />
corresponding to filtered-out samples.<br />
If blocks is not given and the number of genes exceeds \maxBlockSize, genes are preclustered<br />
into blocks using the function consensusProjectiveKMeans; otherwise all genes<br />
are treated in a single block.