sircleRCM_RP
sircleRCM_RP.Rd
Computes the regulatory clustering model (RCM) using the SiRCle regulatory rules for RNAseq and Proteomics data layers (RP).
Usage
sircleRCM_RP(
rnaFile,
protFile,
geneID,
rnaValueCol = "Log2FC",
rnaPadjCol = "padj",
proteinValueCol = "Log2FC",
proteinPadjCol = "padj",
rna_padj_cutoff = 0.05,
prot_padj_cutoff = 0.05,
rna_FC_cutoff = 1,
prot_FC_cutoff = 0.5,
backgroundMethod = "P&R",
OutputFileName = "Sircle_RCM.csv"
)
Arguments
- rnaFile
DF for your RNAseq data (results from DeSeq2 and also your normalised expression counts)
- geneID
Column name of geneId this MUST BE THE SAME in each of your protein, RNAseq and DNAmethylation files (we join on this)
Column name of RNA value in rnaFile
- rnaPadjCol
Column name of RNA p adjusted value in rnaFile
- proteinValueCol
Column name of protein log fold change in proteinFile
- proteinPadjCol
Column name of protein p adjusted value in proteinFile
- backgroundMethod
Optional: Background methods: "P|R", "P&R", "P" , "R", or "*". For details on the methods, please check https://github.com/ArianeMora/SiRCleR/blob/main/vignettes/SiRCle_RCM_Notebook.Rmd Default="P&R"
- proteinFile
DF of your Protein data (results from DeSeq2 and also your normalised expression counts)
- rnaPadjCutoff
Optional: Padjusted cutoff for RNAseq data Default=0.05
- rnaLogFCCutoff
Optional: LogFoldchange cutoff for RNAseq data Default=0.5
- proteinPadjCutoff
Optional: Padjusted cutoff for Protein data Default=0.05
- proteinValueCutoff
Optional: LogFoldchange cutoff for Protein data Default=0.3
- outputFileName
Optional: Output filename Default=SiRCle_RCM.csv