Welcome to synphage Discussions! #16
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My impression. Using a macbook pro M2, OS sequoia 15.0. Installation using conda failed first because dagster complained pkg-config was not present, so I installed that. Then it failed because cairo was no present, so I installed that. Then dagster got up OK and I could go through the many steps required to get to a similarity plot. The blast comparisons of relatively small virus genomes (12-20 kb), and relatively few genomes (26) took much longer than I expected, as in my experience, once the databases have been set up for a blastn or blastp run, then searching such a small database is usually lightning fast. In any case, I finally get to the plot stage and the default format output is far less impressive than say clinker (https://github.com/gamcil/clinker), which gives high quality gene maps and similarity connectors. In clinker I can use an easy interface to alter the output but in synphage I have to play with a config file and run again. For all the extra time needed to set up synphage, and to run the various stages, I am wondering what are the advantages over existing tools, and how can it be made easier and faster to use. |
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