This function takes a tidy dataframe as input containing RNA sequencing data for one or more samples and conducts in-silico repression. Make sure to run with the same arguments for ppi and cache to maintain consistency for a given pipeline.
compute_dnp(
cache = NULL,
df,
experiment_name,
ppi,
ncores = 1,
min_score = NULL
)
data.frame
user-provided filepath for where to store data etc
dataframe output of compute_np
name of the experiment for saving output.
should we use biogrid or stringdb for the PPI
number of cores to use for calculations
if ppi is stringdb, which mininum score should we use to filter edges?