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- 4 months, 1 week ago
Posts by ghahhari.nm
... Thank you Jennifer! Indeed I tried to set the q value which helped a lot and I found a reasonable number of binding events which is different between treatments and it's good! I also tried to follow the Galaxy tutorial by finding the d value first and after peak calling I found very similar results ...
... Hello everyone! Sorry for long explanation! I did paired-end ChIP-seq for my input and IP samples and I used MNase instead of sonication for DNA fragmentation. I have duplicate of each sample. After converting from fastq. to sam files, I merged duplicates of each sample with bamtools and also sorte ...
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