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Thanks for a great program. I’m new at linux and ariba so this might be stupid question. I wonder what is the command for setting spades as the assembler when performing a run.
I thought it was “ariba run [--assembler spades] ref reads_1.fq reads_2.fq output_dir
but I get error argument.
I also wonder if its possible to set a minimum coverage? We experience carryover between some sample when doing multiplexing in Illumina and we get a hit on genes we know are wrong, with few reads (around 5-10) and ctg_cov around 1-2.
Thanks for the help
The text was updated successfully, but these errors were encountered:
Re spades: that command looks correct. What error do you get? But in any case, unless you have a compelling reason for using spades, I recommend using the default assembler instead.
Re min coverage: you can filter the output file on the ctg_cov column, which is the mean read depth across the contig.
Thanks for a great program. I’m new at linux and ariba so this might be stupid question. I wonder what is the command for setting spades as the assembler when performing a run.
I thought it was “ariba run [--assembler spades] ref reads_1.fq reads_2.fq output_dir
but I get error argument.
I also wonder if its possible to set a minimum coverage? We experience carryover between some sample when doing multiplexing in Illumina and we get a hit on genes we know are wrong, with few reads (around 5-10) and ctg_cov around 1-2.
Thanks for the help
The text was updated successfully, but these errors were encountered: