Entering edit mode
8.3 years ago
GK1610
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120
I have a set of chip seq bam files.
I have ~ 24 million paired-end reads in these bam files
I used macs2 for narrow peak calling
macs2 callpeak -t $SAMPLE_1 -c $CONTROL --keep-dup all -f BAMPE -g hs -n $OUTPUT -B -p 1e-3
I am getting only 35K peaks. I expect to see 150-200k peaks. do you have any suggestions?
What the others said, but why do you expect 150-200k peaks?
In general it is not a good idea to call 150-200K peaks, as it will contain many false positive peaks. 35K peaks looks reasonable.
Agree with @Chirag Nepal, but you can change your criteria -p/q value for that.