get_diff | R Documentation |
Differential expression analysis
get_diff( data = NULL, DE_method = "edgeR", normalize_samples = TRUE, threshold_log2foldchange = 2.5, threshold_pval = 0.05, threshold_adjpval = 0.001, k = 1, n_topGenes = 500, parallel_cores = 2 )
data |
The purified profiles of subgoups and control groups for each clinical query sample |
DE_method |
edgeR, DESeq2 or limma DE analysis. |
normalize_samples |
if TRUE, RUVSeq normalization is applied to either EdgeR or DESeq. No normalization needed for limma+voom. |
threshold_log2foldchange |
threshold for log2foldchange. 2.5 by default. |
threshold_pval |
threshold for pvalue. 0.05 by default. |
threshold_adjpval |
threshold for adjusted pvalue. 0.001 by default. |
k |
either k=1 (by default), k=2 or k=3, number of factors used in model matrix construction in RUVSeq normalization if normalize_samples=TRUE. |
n_topGenes |
number of empiricaly differentially expressed genes estimated for RUVSeq normalization. Default is 5000. |
parallel_cores |
number of cores to be used for parallel computing in DESeq2. |
A list with list of differentially expressed genes.
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