dmr_combine_multChrs4rank
This program is used to combine DMR/MRs from multiple chromosomes.
Required Parameters
inChrs
or--in_chroms_number
: A string of chromosomes that need to be combined, separated by commas. For example: chr1,chr2,chr3.inFold
or--in_file_folder
: The file folder containing MR data for each chromosome that is exported by dmr_analysis_block.
Optional Parameters
inSFold
or--in_File_subFolder
: The subfolder of exported MR data in each chromosome based on dmr_analysis_block. Default is “plots” located under each chromosome folder.inMPer
or--in_minimum_percentage_changes
: The minimum percentage of data points in an MR with a predefined methylation change greater than a cutoff. Default is 0.0001.inPC
or--in_Pvalue_cutoff
: The P-value cutoff for the significance test. Default is 0.05.inIsSmd
or--in_is_smoothed_data
: The type of data used for the results: raw = 0, interpolated = 1, or smoothed = 2. Default is 0.inAC
or--in_accuracy_cutoff_range
: The range of clustering accuracy. Default includes all values from 0.0 to 1.0, specified as 0.0,1.1.inDMRst
or--in_DMR_string_type
: A string used to represent predicted DMRs in the file. Default is “D” for predicted DMRs.inLRpb
or--in_LogReg_proba
: A probability value used by logistic regression to select DMRs. Default is 0.8.inMT
or--in_moderate_ttest
: The type of significance test to evaluate: 0 for standard T-test, 1 for moderate T-test, and 2 for KS-test. Default is 0.inLMH
or--in_low_median_high_cutoff
: Use high, median, or low minimum percentage change for DMR ranking. Default is “high”.inFEstr
or--in_file_ending_string
: The file name ending string used to search for result files in the result folder (e.g., chrY/plots/). Default is “_all”.