-
Notifications
You must be signed in to change notification settings - Fork 0
New issue
Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.
By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.
Already on GitHub? Sign in to your account
Issues while anaysing highly similar genomes #6
Comments
(reposting here, as replying to the email seems not to have worked) Hi Manish, |
Hi Leon,
We need to ensure that this is working for all use cases. |
It seems that this issue is caused when pansyri does not like the input file names in the |
I can reproduce the error. It's weird that this only arises when calling core synteny. |
Okay, I think i might have fixed what is happening in c565b85. |
Earlier, it seemed to be working when the filenames were |
I think this commit should fix the need for this filename format (it was hardcoded to match the names in the Ampril dataset). |
Ah, sorry I forgot to test it again after the commit. My account for the HPC at Cologne is expired now, I'll test it again when I get the account renewed. Testing locally, everything works on the ampril dataset, but that's not really a surprise. |
I think there is some incompleteness in the
pansyri.pansyn.find_overlaps
as it is giving me error when I try to get pansyntenic region with two highly similar (actually simulated) query genomes.The files are here:
/srv/netscratch/dep_mercier/grp_schneeberger/projects/syri2/results/human/simulatedgenomes/chr22
We can discuss it when you have some time.
The text was updated successfully, but these errors were encountered: