Sorry that this is a very simple question that might be already posted but I could not find the answers.
I have bacterial metagenomic sequences generated from Illumina HiSeq.
I am done with assembly of short reads and am about to blast them. Since I am new to this field, I am not very clear with the next step.
Q1. For blast, I first used the command below.
formatdb -i input.fasta -p F -o T
It generated several files with different extensions.
Then,
blastall -p blastx -i input.fasta -d my_database -o my_output_file
I guess "-i" is the file I used for formatdb command. What should I use for "-d" as I have several files generated from formatdb command?
Q2. I found that someone uses prokka before blast. I haven't heard about this pipeline but I assume it annotates sequences. Should I use this kind of annotation pipeline before blast?
Thanks for your help in advance!
I have bacterial metagenomic sequences generated from Illumina HiSeq.
I am done with assembly of short reads and am about to blast them. Since I am new to this field, I am not very clear with the next step.
Q1. For blast, I first used the command below.
formatdb -i input.fasta -p F -o T
It generated several files with different extensions.
Then,
blastall -p blastx -i input.fasta -d my_database -o my_output_file
I guess "-i" is the file I used for formatdb command. What should I use for "-d" as I have several files generated from formatdb command?
Q2. I found that someone uses prokka before blast. I haven't heard about this pipeline but I assume it annotates sequences. Should I use this kind of annotation pipeline before blast?
Thanks for your help in advance!
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