Description Usage Arguments Details Value Examples
Counts the number of sequence reads that fall into identically sized bins across the entire genome.
1 | getReadDepth(rdo)
|
rdo |
|
Assumes that the correct directory structure is in place (see full description in copyCat documentation)
In brief, the directory "reads" should be present and should contain read positions in bed format.
returns the original rdObject with the @chrs attribute updated to contain a list of N data frames (one for each chromosome). Each data frame contains one column "rd" containing the counts for each bin.
1 2 3 4 5 | ##create a rdObject, set bin params
# x <- new("rdObject")
##fill the bins with reads
# x.reads <- getReadDepth(x)
|
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.