bt.slop | R Documentation |
Add requested base pairs of "slop" to each feature.
bt.slop(
i,
g,
b = NULL,
l = NULL,
r = NULL,
s = NULL,
pct = NULL,
header = NULL,
output = NULL
)
i |
<bed/gff/vcf> |
g |
<genome> |
b |
Increase the BED/GFF/VCF entry -b base pairs in each direction. - (Integer) or (Float, e.g. 0.1) if used with -pct. |
l |
The number of base pairs to subtract from the start coordinate. - (Integer) or (Float, e.g. 0.1) if used with -pct. |
r |
The number of base pairs to add to the end coordinate. - (Integer) or (Float, e.g. 0.1) if used with -pct. |
s |
Define -l and -r based on strand. E.g. if used, -l 500 for a negative-stranded feature, it will add 500 bp downstream. Default = false. |
pct |
Define -l and -r as a fraction of the feature's length. E.g. if used on a 1000bp feature, -l 0.50, will add 500 bp "upstream". Default = false. |
header |
Print the header from the input file prior to results. |
output |
Output filepath instead of returning output in R. |
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