MACS2 reads report inconsistent with samtools flagstat
Hi there,
But, I am still confused.
My IP bam flagstat:
18880801 + 0 in total (QC-passed reads + QC-failed reads)
253218 + 0 duplicates
14130154 + 0 mapped (74.84%:-nan%)
0 + 0 paired in sequencing
0 + 0 read1
0 + 0 read2
0 + 0 properly paired (-nan%:-nan%)
0 + 0 with itself and mate mapped
0 + 0 singletons (-nan%:-nan%)
0 + 0 with mate mapped to a different chr
0 + 0 with mate mapped to a different chr (mapQ>=5)
MACS2 report:
# tag size is determined as 36 bps
# total tags in treatment: 8308438
# tags after filtering in treatment: 8005485
# maximum duplicate tags at the same position in treatment = 1
# Redundant rate in treatment: 0.04
So, after remove duplicates:
14130154 (mapped) - 253218(duplicates) = 13876936.
This number is still much bigger than 8308438.
So, why is that? and why MACS2 further filter down to 8005485?
Thanks,
Ming
• 3,654 views
•
link
0 answers
No answers yet.
Log in to answer this question.
It might be that macs2 removes reads with mapq below a certain threshold and other uncertain reads. Try to run
samtools view -c -F3844 -q 5 myaln.bamand see if you get a number closer to macs'.-F3844filters out:Thanks for your comment. but MACS2 does not check read quality: https://groups.google.com/forum/#!topic/macs-announcement/ASQ3GsXQC1c
I run that command, and it gives me 14,130,154
Still much bigger than the 8 million reads MACS2 retains.