Description Usage Arguments Details Value
View source: R/accessory_funcs.R
Subsets a given list of CpGs by another list of CpGs
1 2 3 4 5 6 7 8 9 10 11 |
chr_idx |
integer; column of the chromosome |
start_idx |
integer; column of the CpG start site |
end_idx |
integer; column of the CpG end site |
strand_idx |
integer; column of the strand |
beta_idx |
integer; column of the beta value |
M_idx |
integer; column of the # of methylated reads |
U_idx |
integer; column of the # of unmethylated reads |
cov_idx |
integer; column of the coverage |
verbose |
flag to output messages or not |
Typically used to reduce the number of potential CpG sites to include only those present in the input files so as to maximize performance and minimize resources. Can also be used for quality control to see if there is excessive number of CpG sites that are not present in the reference genome.
List of column names and indexes
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.