View source: R/DESeq2_functions.R
get_Results_DDS | R Documentation |
When running DESeq2 you usually add multiple terms to the matrix design. Test the effect of them
get_Results_DDS(
dds_object,
OUTPUT_Data_dir_given,
dfAnnotation,
list_of_cols,
comp_ID,
sign_value.given = 0.05,
LFC.given = log2(1.2),
int_threads = 2,
coef_n = NA,
forceResults = FALSE,
min_cutoff_to_plot = 3,
max_cutoff_to_plot = 50,
gene.annot = NULL,
data_type = "mRNA",
shrinkage.given = "apeglm"
)
dds_object |
DESeq2 object (DESeqDataSet) |
OUTPUT_Data_dir_given |
Absolute path to store results |
dfAnnotation |
Dataframe with useful metadata to include |
comp_ID |
Tag name to include for each comparison |
sign_value.given |
Adjusted pvlaue cutoff. Default=0.05, |
LFC.given |
Log Fold change cutoff. Default=log2(1.2), |
int_threads |
Number of threads to use in the analysis |
coef_n |
Number of the coefficient of results to test (if desired) |
forceResults |
Boolean to force re-run analysis if already generated in the folder provided |
min_cutoff_to_plot |
Minimun number of genes significant to continue analysis. Default=3 |
max_cutoff_to_plot |
Number of genes significant to plot as candidates analysis. Default=50 |
gene.annot |
Dataframe containing gene annotation (Default: NULL) |
shrinkage.given |
LFC shrinkage estimator provided. Available: apeglm, ashr or normal |
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