Identify significant chromatin interations for multiple chromosome conformation capture assays
1 2 3 4 5 6 | limacc(fragment_file, contact_file, dtype = "CHiC",
peakFile4HiChIP = NULL, out_filename = "sigRes.txt",
comb_rep = "merge", numG = 100, hcrc = 0.9, fdr = 0.1,
nIter = 20, maxN = 10000, minLen = NULL, maxLen = NULL,
minDist = 1000, maxDist = 2 * 10^6, adj.method = "IHW",
adj.sdepth = NULL, updateMethod = "smooth")
|
fragment_file |
the name of restriction enzyme file for CHiC/CC or binned fragment_file for HiChIP |
contact_file |
contact map file(s) |
dtype |
data type, CHiC/CC/HiChIP |
peakFile4HiChIP |
file of coordinate of 1D peak (bed file or similar format) for HiChIP, NULL for other type of data |
out_filename |
output file name |
comb_rep |
if length(contact_file)>1, merge or pool replicates (default merge for CHiC; pool for HiChIP) |
numG |
number of groups for limacc (default 100) |
hcrc |
initial guess of backgound proportion (default 0.9) |
fdr |
fdr cutoff used for the final output (default 0.05) |
nIter |
maxmimum number of iterations (default 20) |
maxN |
filter contacts that wiht more than maxN counts (default 10000) |
minLen |
filter otherEnd fragments with length smaller than minLen |
maxLen |
filter otherEnd fragments with length greater than maxLen |
minDist |
minimum distance in bp, default 1000bp |
maxDist |
maximum distance in bp, default 2Mb |
adj.method |
method for adjusting p-value (default 'IHW') |
adj.sdepth |
the number (in million) to which the sequence depth should be normalized, default NULL means do not adjust the total sequence depth |
updateMethod |
smooth or noupdate (default 'smooth') |
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