Hi all,
Can any one help me in resolving this issues.
While creating the Tag directory I got this problem.
!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
Average reads per BED file: 255.0
Good chance that the 5th column of your BED file has a weird value in it!
By default, this is read as the number of reads for that position
To count each entry as only one read (ignore the 5th column) use -forceBED
!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
Optimizing tag files...
Optimizing single genome.tags.tsv file...
Estimated genome size = 2911405191
Total Tags = 6130413690.0
Total Positions = 17702615
Average tag length = 50.0
Median tags per position = 255 (ideal: 1)
Average tags per position = 346.300
!! Might have some clonal amplification in this sample if sonication was used
If this is ChIP-Seq using sonicated fragments, consider adding the option "-tbp 1"
Ignore if analyzing RNA, MNase, etc. data
Fragment Length Estimate: 103
Peak Width Estimate: 10
!!! No reliable estimate for peak size
Setting Peak width estimate to be equal to fragment length estimate
Autocorrelation quality control metrics:
Same strand fold enrichment: 1.1
Diff strand fold enrichment: 1.1
Same / Diff fold enrichment: 1.0
Guessing sample is ChIP-Seq - may have low enrichment with lots of background
When I tried fixing it using force5th I am still getting the same error and I am not getting the Autocorrelation properly while doing the plot.
Thanks
1 answer
Hi
The issue is I am not getting the autocorrelation image as its generated in HOMER.
Instead of a distribution plot which gives relative distance between the reads generated through HOMER, I am getting a perpendicular line.
When I checked the values in the tagAutocorrelation.txt file I found at 0th position under ( Distance in bp(Fragment Length Estimate: 120)(Peak Width Estimate: 120)) the values for the in the Same strand and opposite strand is 4739956.0 137976.0 respectively.
Generally the Same strand value is 0 with the kind of analysis I have done so far.
So why I am getting this huge value?
Secondly When I removed this value and made it 0, I could generate the correlation plot.
Why is it coming like this.
Thanks
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from your question it is not clear what you think that the problem is
Hi
The issue is I am not getting the autocorrelation image as its generated in HOMER.
Instead of a distribution plot which gives relative distance between the reads generated through HOMER, I am getting a perpendicular line.
When I checked the values in the tagAutocorrelation.txt file I found at 0th position under ( Distance in bp(Fragment Length Estimate: 120)(Peak Width Estimate: 120)) the values for the in the Same strand and opposite strand is 4739956.0 137976.0 respectively.
Generally the Same strand value is 0 with the kind of analysis I have done so far.
So why I am getting this huge value?
Secondly When I removed this value and made it 0, I could generate the correlation plot.
Why is it coming like this.
Thanks