basecountimport: Import SBC (basecounts) Given Coordinate File

Description Usage Arguments See Also

Description

Calculates the SBC (basecounts) from a specified basecount file for a given set of merged significant windows, given a threshold level and the results from getsigwindows().

Usage

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basecountimport(inputfile,winlist,threshold=.01,method='pscl',printFullOut=0,
    outputfile,twobitfile,chromosome='all'

Arguments

inputfile

path to basecount track containing SBPC information for the entire genome, generated by basealigncount()

winlist

path to files outputted from getsigwindows()

outputfile

path to where file of extracted basecounts should be placed

chromosome

which chromosomes in coordinate file to get basecounts for. Default is all.

threshold

threshold for signfiicant windows corresponding to method used (mixture vs pscl)

printFullOut

specifies the file format ouputted from getsigwindows, where 1 correspondinds to output of full dataset with posterior enrichment probability results, 0 corresponds to only genomic coordinates and posterior probabilities

method

method used to generate files in winlist, either mixture or pscl

twobitfile

path to current build of human genome in .2bit format

outputfile

specify file name/path for temporary file that holds matrix of overlap information generated for peak refinement

See Also

save.


sivarajankumar/zinba documentation built on May 29, 2019, 10:11 p.m.