Entering edit mode
Hi Joel,
The mailing list will not distribute large attachments, so we can't
see
your code script.
Most likely you've made an error in the script, because the classic
and
glm pipelines in edgeR should give very similar results for a two
group
comparison. We would need to see the code to tell what the error is.
We
shouldn't need to see your data, just the code.
Best wishes
Gordon
--------- original message -----------
Jiantao Yu joelyu.2003 at gmail.com
Thu Dec 12 22:54:05 CET 2013
Dear Sir/Madam,
When I used edgeR to do RNA-Seq analysis, I found the datasets of the
resulting DEGs generated by 'Classic' and 'GLM' methods are very
different,
the former contain ~460 DEGs, whereas the latter generate ~27,000
DEGs. I
don't know why this was happening. I attached the scripts and the
source
data I used, hope you would help me to explain this.
Joel
-------------- next part --------------
"mu1.bam" "mu2.bam" "mu3.bam" "wt1.bam" "wt2.bam" "wt3.bam"
"AT1G01010" 50 89 54 69 71 56
"AT1G01020" 218 261 198 309 248 241
"AT1G01030" 27 47 26 50 48 23
"AT1G01040" 582 676 466 202 229 830
"AT1G01046" 10 11 8 6 6 5
...
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