View source: R/normalize_filter.R
hpgl_filter_counts | R Documentation |
This is identical to cbcb_filter_counts except it does not do the somewhat tortured log2CPM() but instead just uses a 4 cpm non-log threshold. It should therefore give basically the same result, but without the shenanigans.
hpgl_filter_counts(
count_table,
threshold = 2,
min_samples = 2,
libsize = NULL,
...
)
count_table |
Data frame of (pseudo)counts by sample. |
threshold |
Lower threshold of counts for each gene. |
min_samples |
Minimum number of samples. |
libsize |
Table of library sizes. |
... |
Arguments passed to cpm and friends. |
Dataframe of counts without the low-count genes.
[edgeR]
## Not run:
filtered_table <- cbcb_filter_counts(count_table)
## End(Not run)
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