Description Usage Arguments Details Examples
This will perform differential expression using edgeR for pairwise comparisons
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| input | Input expression set | 
| pd | pData, optional, by default set to pData of input | 
| DEgroup | a pData variable | 
| contrastID | the condition value from DEgroup to be used as the contrast | 
| sizefactor | a pData column containing the scran reported size factor for each cell | 
| lib_size | a pData column containing the library size for each cell | 
| facet_by | a pData variable to iterate through and perform DE for a condition within each group | 
| minCells | minimum cell fraction the genes should be expressed in to be tested for DE | 
| batchID | a pData variable to use for model accounting for batch effects | 
| outdir | an output directory | 
| outsuffix | an output file suffix | 
| pVal | pvalue cutoff for reported results, by default reports all results | 
| contrast | a list of contrasts to be used for the DE analysis, default is a two-class comparison, with the second class as the comparison class | 
Utilize information stored in pData to control the DE performed
| 1 | findDEgenes(input, pd = selected_table, DEgroup = "genotype", batchID = "beads", facet_by = "cluster", sizefactor="sizefactor", lib_size="lib_size")
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