View source: R/runDEAnalysis.R
Run Analysismethods
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working.dir |
Input file location |
output.dir |
Result file location |
real |
A logical indicating whether this analysis is for synthetic data or real data. Possible values are TRUE or FALSE. |
fpc |
A logical indicating whether simulation data is made from a single sample group (e.g. normal) to calculate False positive counts. Possible values are TRUE or FALSE. Only used for real data analysis. |
data.types |
A vector indicating types of dataset (e.g. data.types = c(KIRC, Bottomly, mBdK and mKdB)) |
fixedfold |
A logical indicating whether simulation data is made from fixed fold to imitate SEQC counts data. Possible values are TRUE or FALSE. Only applied if this simulation is synthetic data simulation. |
rep |
An integer specifying iterations each test perform. |
nsample |
A vector indicating number of samples. |
nDE |
A vector indicating number of generated DE genes in the synthetic data. |
fraction.upregulated |
A vector specifying proportion of upregulated DE genes in the synthetic data. Default value is 0.5. (e.g. fraction.upregulated = c(0.5, 0.7 and 0.9)) This vector is available only if fixed fold is FALSE. |
disp.Types |
A vector indicating how is the dispersion parameter assumed to be for each condition to make a synthetic data. Possible values are 'same' and 'different'. |
modes |
A vector specifying test conditions we used for simulation data generation. "D" for basic simulation (not adding outliers). "R" for adding 5 "OS"for adding outlier sample to each sample group. "DL" for decreasing KIRC simulation dispersion 22.5 times (similar to SEQC data dispersion) to compare with SEQC data. |
AnalysisMethods |
A vector specifying DEmethods used for the analysis. (e.g. 'edgeR','edgeR.ql','edgeR.rb','DESeq.pd','DESeq2','voom.tmm','voom.qn','voom.sw','ROTS','BaySeq','BaySeq.qn,'PoissonSeq','SAMseq') |
para |
A list parameter consists of multiple lists corresponding each method. Each method list contains multiple parameters to run each DE analysis method. |
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