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Hello, our data is a fasta file with a size of 1343M and 5.25 million predicted proteins. We use run.sh and default settings to perform ARG identification. We found that the program first splits the files into individual sequences in onn4argtmp/work/, and then runs them sequentially. We only completed 3782 sequences in one day. May I ask if there is a way to speed up the operation, or if there was an error in our steps?
The text was updated successfully, but these errors were encountered:
Hello, our data is a fasta file with a size of 1343M and 5.25 million predicted proteins. We use run.sh and default settings to perform ARG identification. We found that the program first splits the files into individual sequences in onn4argtmp/work/, and then runs them sequentially. We only completed 3782 sequences in one day. May I ask if there is a way to speed up the operation, or if there was an error in our steps?
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The text was updated successfully, but these errors were encountered: