Dear all,
I am trying to run SICER on my files. I have done a bamToBed conversion and concatanated the files with cat.
Command looks like:
SICER.sh . merged.bed ctl.bam.bed . mm10 1 200 50 0.83 600 0.01
What Sicer does is it produces two big "removed" files and all the other files are empty. and no bedfiles.
this is the out:
m   Plus reads: 0   Retained plus reads: 0 ;    Minus reads: 0  Retained minus reads: 0
m   Plus reads: 0   Retained plus reads: 0 ;    Minus reads: 0  Retained minus reads: 0
1   Plus reads: 21272531    Retained plus reads: 18711806 ; Minus reads: 21284872   Retained minus reads: 18718548
0   Plus reads: 18979534    Retained plus reads: 16908229 ; Minus reads: 19025034   Retained minus reads: 16934977
_   Plus reads: 0   Retained plus reads: 0 ;    Minus reads: 0  Retained minus reads: 0
c   Plus reads: 0   Retained plus reads: 0 ;    Minus reads: 0  Retained minus reads: 0
h   Plus reads: 0   Retained plus reads: 0 ;    Minus reads: 0  Retained minus reads: 0
r   Plus reads: 0   Retained plus reads: 0 ;    Minus reads: 0  Retained minus reads: 0
o   Plus reads: 0   Retained plus reads: 0 ;    Minus reads: 0  Retained minus reads: 0
m   Plus reads: 0   Retained plus reads: 0 ;    Minus reads: 0  Retained minus reads: 0
s   Plus reads: 0   Retained plus reads: 0 ;    Minus reads: 0  Retained minus reads: 0
No idea what m,c,r,h etc. reads are..
Hi, Indeed there was a problem with the genomedata.py. As you see the chromosomes spell our mm10-chroms :) thanks!