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Q: Stuck with initialisation of a workflow (atac-seq) #941
Comments
Thanks for the issue, I'll take a look. Probably after the weekend I have an answer for you |
Could you post what's in this file: On what kind of computer are you running it? Linux, Mac, or Windows? |
Thanks for your very quick response!! We are running it on a Mac, 4 cores. 32gb mom |
I can't reproduce the error, but I think it's because mac has a different version of grep than linux. Could you add grep to the environment that's needed for the trackhub index? That's file:
And then run seq2science as you normally would. It should re-install the environment, with GNU grep added, and hopefully this works then 😄! Let me know if that solves the issue for you. As a last resort solution you can always set |
Hey! Thanks for that! I had to set the create_trackhub to false... |
It’s the same as #939 (comment) I think. It just so happened we got two Mac users in the span of two weeks!
You either have to update your bedtools environment like the way I say in the link, or turn off the deeptools plots for qc: deeptools_qc: false
I just started my Xmas break, and I will release a new version of seq2science when I’m back with the fixes for both of your issues, so you (and others) don’t have to play with the envs seq2science installs.
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Hey! Thanks already for all your help! but I don't see what is changed to overcome this issue. Kind regards, |
Can you post the log of the actual rule that fails?
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Next time I'll immediately include that! |
That one I actually solved yesterday (I think). At the end of today there will be a new seq2science release. Hopefully everything works for you with that version |
You can try |
The issue you had was with conda and the newest numpy version. I've changed the description on which numpy version should be used on the bioconda side, so probably removing the environment and just restarting the run with the current seq2science version also works btw.
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I'm assuming this has been resolved, feel free to reopen if not |
Question
We are trying to analyze atacseq data from 36 samples. As a trial I wanted to test if this workflow would work on f.e. the first four samples. of which the first three are biological repeats. I can start the workflow, but I simply don't understand the error I get...
What have I tried
Here you can find the config and samples file (I had to convert them to .txt to be able to upload it here. I also screenshotted the folder structure. Thanks in advance!!!
seq2science.2022-12-16T153021.745497.log
samples.txt
config.txt
s://github.com/vanheeringen-lab/seq2science/files/10246660/samples.txt)
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