Entering edit mode
3.9 years ago
pt.taklifi
▴
60
hello everyone ,
I am analyzing fastq files on galaxy. I aligned fastq files to hg38 reference genome using bowtie2
and produced BAM
files. now I want to remove alpha satellite repeats, Alu repeats, ribosomal DNA repeats, and other repeat regions. I think -k 1 -D 20 -R 3 -N 1 -L 20 -i S,1,0.50 -X 2000 –rg-id
options in bowtie2
removes these repeats however I'm not sure how to do this task on galaxy
I would appreciate your help
Hi, do you mean specific elements or just repetitive regions where reads will not uniquely map in general? If you want to remove multimappers then filtering for a MAPQ using
samtools view
(the-q
option) might do the trick very easily.Please ask on Galaxy help forum here: https://help.galaxyproject.org/
install bowtie2 as admin and check if these options are available under advanced options.