Differential Expression Results Tables
resultsTables(object, ...) # S4 method for DESeqResults resultsTables(object, lfc = 0, write = TRUE, summary = TRUE, headerLevel = 3, dir = file.path("results", "differential_expression"), organism = NULL, quiet = FALSE)
| object | Object. |
|---|---|
| ... | Additional arguments (for the S4 generic definition). |
| lfc | Log fold change ratio (base 2) cutoff. Does not apply to
statistical hypothesis testing, only gene filtering in the results tables.
See |
| write | Write CSV files to disk. |
| summary | Show summary statistics as a Markdown list. |
| headerLevel | Markdown header level. |
| dir | Directory path where to write files. |
| organism | Optional. Override automatic genome detection. By default the function matches the genome annotations based on the first Ensembl gene identifier row in the object. If a custom FASTA spike-in is provided, then this may need to be manually set. |
| quiet | If |
Results list.
data(res) resTbl <- resultsTables(res, lfc = 0.25, write = FALSE)#> #>#>#> #> #> ### Summary statistics #> #> #> - 505 genes in count matrix #> - base mean > 0: 304 genes (non-zero) #> - base mean > 1: 213 genes #> - alpha cutoff: 0.1 #> - lfc cutoff: 0.25 (applied in tables only) #> - deg pass alpha: 4 genes #> - deg lfc up: 2 genes #> - deg lfc down: 2 genes #>class(resTbl)#> [1] "list"names(resTbl)#> [1] "contrast" "alpha" "lfc" "all" #> [5] "deg" "degLFC" "degLFCUp" "degLFCDown" #> [9] "allFile" "degFile" "degLFCUpFile" "degLFCDownFile"