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How to run this tool? #13
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That's funny - someone else forked this repo about a year ago, refactored and submitted to pypi as viral_verify (https://github.com/peterk87/viral_verify) . That's why the output and such is so different. Thanks for pointing that out! Meanwhile, our current github version is awaiting approval for bioconda channel. As soon as that happens, I'll update accordingly. |
That is so weird. They also took the namespace too? What's the process like for getting something on bioconda? |
That's open source, after all... |
Hi there, so in the end which database did you use or is that one annotated out a bit more accurately. |
I use geNomad now. |
All right, thanks. |
Apologies @AndAvia , I wrote that from my phone but should have given more context. Here's the geNomad publication: https://www.nature.com/articles/s41587-023-01953-y and here's the GitHub: https://github.com/apcamargo/genomad I developed a wrapper around geNomad for my "binning-viral" module (though, it doesn't really bin and more so identifies contigs that are viral) in my VEBA package. Here's the publication for VEBA (https://academic.oup.com/nar/advance-article/doi/10.1093/nar/gkae528/7697622) and here's the GitHub (https://github.com/jolepsin/veba). If you only want to perform viral analysis, I would recommend just using geNomad because VEBA has a lot of functionality in other modules (e.g., assembly w/ SPAdes, rnaSPAdes, Fly or eukaryotic binning/gene modeling, etc) and requires more dependencies/databases. |
@jolespin Thank you so much for your patience in replying! I only need to do virus identification at the moment, because there are so many virus identification software, I'm going to use genomad, VIBRANT, virfinder, deepvirfinder, virsorter, virsorter2, ViralVerify and these, but you said that ViralVerify two databases have different results, and I don't know which database to choose.I had a chance to look at your VEBA, and I found it very impressive! Wishing you a wonderful day! |
Hi, |
I'm working on an institute-wide pipeline for JCVI and had some trouble running your tool.
Here's my version installed via pip:
Here's my command:
Edit: I had to decompress the PFAM database which was the error in the original post that I've edited since then.
Should I be using the PFAM database or the database from FigShare?
Can you update the Usage on your GitHub?
This is the results output:
I ran the version from GitHub on a differen tdataset and got the following output:
How come the output is so different between the pip and GitHub versions?
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