Description Usage Arguments Value Author(s) Examples
Compute the number of reads overlapping the specified positions for a single chromosome.
1 | bindcount.chr(tagdat, bindpos, fragL = 200, whs = 250)
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tagdat |
A numeric vector of the genome coordinates for the starting positions of the aligned reads, with positive numbers representing the 5' strand and negative numbers representing the 3' strand. |
bindpos |
A numeric vector of the genome coordinates whose numbers of covering tags are computed. |
fragL |
A numeric value for the fragment length of the sequencing reads. Default: 200. |
whs |
A numeric value for the half window size around the binding position. All tags overlapping this region are counted. Default: 250. |
A numeric vector of the numbers of reads overlapping each position corresponding to "bindpos".
Chandler Zuo zuo@stat.wisc.edu
1 2 3 | data( tagdat_chip )
data( bindpos )
bindcount.chr( tagdat_chip[[1]], bindpos[[1]], fragL = 100, whs = 300 )
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