Dear bioc-sig-sequencing,

If I run BioC2010 lab example, 
http://www.bioconductor.org/help/course-materials/2010/BioC2010/Workflow.pdf, I 
get the 184 to 196 bp average fragment length, as indicated on page 3 for 
"ctcf" sample.

If run same code on some of my own chipseq Arabidopsis samples (Eland-aligned 
"export" files), for some, get average fragment length of approximately 86 bp, 
for others get approximately 70 bp.  Submitters of these samples believe the 
average fragment length for these sonicated samples is in the range of 200-250 
bp.

Looking at the ref paper for how the SISSR algorithm works (Jothi et al., NAR 
36 5221 2008), it looks like fragment length estimate not affected by what DNA 
binding protein one may be studying, thus, perhaps fairly straight forward 
calculation.

So how to proceed?  Perhaps just resize to the length found by the 
estimate.mean.fraglen chipseq function, and proceed to analyze for which peaks 
are different in two samples?

Or is there an alternative option one should consider with the seemingly too 
short average fragment length calculation results?


Thanks,
P. Terry
[email protected]

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