Comments (3)
from fithic.
Hi,
Thank you for your reply.
I ran Fithic2 without biases file, and it gives me the results:
However, I want to run it with a biases file. Keeping your comment in mind, I checked the biases file and also created new biases file using HiCKRy.py with HiC-Pro interactions and fragments.
I also filtered the biases with awk '{if ($3 > 0){ print}}'| awk '{if ($3 < 2){ print}}' and fragments with awk '{if ($5 > 0){print }}'
I used these files to run fithic2. However, it gives me the same results and all the loci were again discarded.
Could you please tell me how to fix the biases file? I appreciate any suggestions regarding this issue.
I am looking forward!
Many thanks for considering my request.
Best,
Nisar
from fithic.
Seems like there is an issue with your normalization. Maybe about its convergence or maybe about how your reads are distributed. Could you plot coverage tracks per each bin across the genome and/or look at a histogram of coverage (reads per bin)? Bias vector should be normally distributed around 1 (with a mean 1) for FitHiC to work reasonably.
from fithic.
Related Issues (20)
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from fithic.