Description Usage Arguments Details Value
View source: R/experiment_plots.R
Normalizes per position per gene by this function: (reads at position / min(librarysize, 1) * number of genes) / fpkm of that gene's RNA-seq
1 | rnaNormalize(coverage, df, dfr = NULL, tx, normalizeMode = "position")
|
coverage |
a data.table containing at least columns (count/score, position), it is possible to have additionals: (genes, fraction, feature) |
df |
an ORFik |
dfr |
an ORFik |
tx |
a |
normalizeMode |
a character (default: "position"), how to normalize library against rna library. Either on "position", normalize by number of genes, sum of reads and RNA seq, on tx "region" or "feature": same as position but RNA is split into the feature groups to normalize. Useful if you have a list of targets and background genes. |
Good way to compare libraries
a data.table of normalized transcripts by RNA.
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