python longpass/LongPass.py -o outcluster/out_cluster.txt --clustering paraclu --normalization raw --params longpass/params.txt --replicate --bamfile sequinB_rep1.trimmed.sort.bam sequinB_rep2.trimmed.sort.bam
You can adjust parameters in params.txt file:
example of parameter file:
powerlaw:
value_range = [10,1000]
distclu:
maxdist = 20
paraclu:
minStability = 1
maxLength = 500
removeSingletons = True
keepSingletonAbove = 15
reducetoNoneoverlap = True
bam
lrtsp
range
1-base file.
first column: chromosome
second column: position
third column: strand
fourth column: TSS count at this position
fifth column: TES count at this position
chrIS 77834 + 29 0
chrIS 90912 + 12 0
chrIS 94351 + 114 0
first column: chromosome
second column: position
third column: strand
fourth column: TSS/TES count at this position
chrIS 77834 + 29
chrIS 90912 + 12
chrIS 94351 + 114
example of output file:
0-base file
chrIS + 2298169 2298173 2 2298169 190.0 200.0 3.33333 0.07033 tss SRR13057605.7787,SRR13057605.1473
chrIS + 4771512 4771514 2 4771512 16.0 29.0 13.0 11.23858 tss SRR13057605.525671,SRR13057605.1473
chrIS + 4778059 4778062 3 4778059 90.0 217.0 63.5 29.96 tss SRR13057605.412450,SRR13057605.1473
chrIS + 3998391 3998466 9 3998465 61.0 198.0 1.6875 0.13665 tss SRR13057605.436442,SRR13057605.1473
chrIS + 4777903 4777908 4 4777907 109.0 249.0 35.0 30.07874 tss SRR13057605.1332445,SRR13057605.91742,SRR13057605.1473
first column: chromosome
second column: gene strand
third column: cluster start site
fourth column: cluster end site
fifth column: peak number in cluster
sixth column: dominant site in cluster
seventh column: number of reads at dominant site
eighth column: number of total reads in the cluster
ninth column: max density of the cluster
tenth column: min density of the cluster
11st column: tss/tes
12nd column: reads ids assign to this cluster