Description Usage Arguments Value Author(s) Examples
Compute the number of aligned reads overlapping the specified peak intervals for the whole genome.
1 |
chipdat |
A list of the starting positions of the ChIP sample aligned reads for each chromosome. The sign of each coordinate represents its strand direction, with a positive numbers on the 5' strand and a negative numbers on the 3' strand. |
inputdat |
A list of the starting positions of the input sample aligned reads for each chromosome. The sign of each coordinate represents its strand direction, with a positive numbers on the 5' strand and a negative numbers on the 3' strand. |
peakpos |
A list containing the genome coordinates for each peak interval on each chromosome. Each list component is a 2-column matrix containing the left and right boundary of the peak intervals on one chromosome. |
fragL |
A numeric value of the fragment length of the aligned reads. Default: 200. |
unique |
A logical value for whether only reads mapping to unique nucleotide positions are counted. |
A list of the numbers of reads that overlap the corresponding peak intervals.
Chandler Zuo zuo@stat.wisc.edu
1 2 3 4 | data( peakpos )
data( tagdat_input )
data( tagdat_chip )
peakcount( tagdat_chip, tagdat_input, peakpos, fragL = 100 )
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