Closed Smiriti-Gupta closed 1 year ago
Hello Sir, Thank You for the response. Yes, I am using the same standalone version as what is run on the web server (version 1.8.0). I am using this tool to identify CRISPR-Cas systems in Metagenome Assembled Genomes (MAGs).The tool identifies CRISPR-Cas systems in a particular bin through web server but no CRISPR-Cas are identified for the same bin using the standalone version. I also have certain other queries mentioned below:
I will be greatful for a quick response. Thank You Smiriti Gupta
On Fri, 6 Jan 2023 at 14:18, Jakob Russel @.***> wrote:
I need a bit more information to figure out where the problem could be.
- Are you using the same standalone version as what is run on the webserver?
- In which way are the results different?
- Do you have a reproducible example I can use for testing?
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Hi I will answer point by point. As for the difference between web server and standalone, how specifically are the outputs different? Do you use some non-default parameters on either the standalone or webserver?
1) You could put them all in one fasta and run cctyper with --prodigal meta
, but it's faster to parallelize across MAGs with for example GNU parallel
2) There is a Cas9 HMM that matches both II-A and II-C, hence it's ambiguous
3) Not sure what you mean by a false positive column?
4) Unknown gene means that it is not CRISPR-Cas related
5) It's an operon with two cas9, or maybe it should have been one gene but the ORF was called wrongly
6) That sounds like a mistake, could you send one of the figures? Also, is it only for specific subtypes or for different subtypes?
Cheers, Jakob
Please find the image showing Cas1 in purple. It is for all subtypes
The Cas1 gene has the expected color. All adaptation related genes will have this color (blur, purple, or what you want to call it).
I need a bit more information to figure out where the problem could be.