metevalue.methylKit {metevalue} | R Documentation |
Calculate E-value of the methylKit data format
Description
Calculate E-value of the methylKit data format
Usage
metevalue.methylKit(
methyrate,
methylKit.output,
adjust.methods = "BH",
sep = "\t",
bheader = FALSE
)
Arguments
methyrate |
is the data of methylation rates of each sites and group. For example:
The columns are (in order): - chr: Chromosome - pos: int Position - g1~g2: methylation rate data in groups | |||||||||||||||||
methylKit.output |
is the output data with e-value of each region - chr: Chromosome - start: The positions of the start sites of the corresponding region - end: The positions of the end sites of the corresponding region - strand: Strand - pvalue: The adjusted p-value based on BH method in MWU-test - qvalue: cutoff for qvalue of differential methylation statistic - methyl.diff: The difference between the group means of methylation level | |||||||||||||||||
adjust.methods |
is the adjust methods of e-value. It can be 'bonferroni', 'hochberg', 'holm', 'hommel', 'BH', 'BY' | |||||||||||||||||
sep |
seperator, default is the TAB key. | |||||||||||||||||
bheader |
a logical value indicating whether the input_filename_b file contains the names of the variables as its first line. By default, bheader = FALSE. |
Value
a dataframe, the columns are (in order):
- chr: Chromosome
- start: The positions of the start sites of the corresponding region
- end: The positions of the end sites of the corresponding region
- q-value: The adjusted p-value based on BH method in MWU-test
- methyl.diff: The difference between the group means of methylation level
- CpGs: The number of CpG sites within the corresponding region
- p : p-value based on MWU-test
- p2: p-value based on 2D KS-test
- m1: The absolute mean methylation level for the corresponding segment of group 1
- m2: The absolute mean methylation level for the corresponding segment of group 2
- e_value: The e-value of the corresponding region
Examples
data(demo_methylkit_methyrate)
data(demo_methylkit_met_all)
## example_tempfiles = tempfile(c("rate_combine", "methylKit_DMR_raw"))
## tempdir()
## write.table(demo_methylkit_methyrate, file=example_tempfiles[1],
## row.names=FALSE, col.names=TRUE, quote=FALSE, sep='\t')
## write.table(demo_methylkit_met_all, file=example_tempfiles[2],
## sep ="\t", row.names =FALSE, col.names =TRUE, quote =FALSE)
## result = metevalue.methylKit(example_tempfiles[1], example_tempfiles[2],
## bheader = TRUE)
## str(result)