extract log fold change information from a list of DESeqResults, return a tibble
1 |
res_list |
a list of DESeqResults, must have the same length |
gene_list |
a list of gene that you want to subset. If you don't provide this, by default this function will return all the gene from DESeqResults |
col_name |
a character vector that gives column name of the output |
... |
other parameters can be used in res_subgroup function reg_dir gives which regulation direction you want to subset you gene three options: all – up and down up – only up regulated down – only down regulated default is all alpha the significant level for adjusted P-value, default is 1, i.e. no alpha requirement reg_LFC reg gives the regulation level change in log2 fold change in absolute value default is 0, i.e. no LFC requirement |
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