Comments (1)
Hi Stefano, unfortunately that cannot be done, as it only made sense to run DIAMOND against large sequence sets to take advantage of the speed gain. Therefore, each proteome is scanned twice: i) against itself and ii) against all others, and thus when using the -I flag the "others" set changes and needs to be recomputed, BRuno
from get_homologues.
Related Issues (20)
- Invalid protein cluster files generated by get_homologues-est when .faa and .fna have genes in different order. HOT 4
- Error with FNA and FAA sequence order HOT 6
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- Error: find_COGs HOT 6
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- Issue with Input files not being detected by Get_homologues HOT 6
- maybe a bug in annotate_cluster.pl HOT 2
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from get_homologues.