I got multiple genomes for different gram-negative bacteria. What program could I use to identify specific core genes under negative selection but with smaller regions that exhibit positive selection? Is there any limitations/problems I might encounter along the way?
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Do you have annotated genomes? Or just the assemblies?
If you have annotations, your project is quite similar to one project I'm working on right now...
My strategy is:
blast all genes vs each other
use R to look for gene clusters (then, you can apply the thresholds you want to decide whether a cluster has to be reported or not...)
If you don't have annotations, I would do more or less the same, instead that I would first try to make annotations using a software like glimmer...
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The recent pandemic caused worldwide health, economic, and social disruptions with its reverberations still felt today. A key takeaway from this event is the need for accurate and accessible tools for detecting and tracking infectious diseases. Timely identification is essential for early intervention, managing outbreaks, and preventing their spread. This article reviews several valuable tools employed in the detection and surveillance of infectious diseases.
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