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⚠️ All reads in the forward and reverse reads files must be in pair and their orders in the two files must be the same. -
The sizes of the output files might be slightly smaller than the input files, which might due to the shorter length of read names in the output files.
You can use
wc -l input_R1.fasta
andwc -l output_R1.fasta
to get the number of lines in the input and output files and see if the numbers are the same.
You can also usehead R1.fasta
ortail R1.fasta
to print on the screen the first/last few lines of a file.
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In fasta format
MarkerMAG rename_reads -r1 R1.fasta -r2 R2.fasta -p soil -t 2
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In fastq format
MarkerMAG rename_reads -r1 R1.fastq -r2 R2.fastq -p soil -fq -t 2
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[prefix]_R1.fasta
>[prefix]_1.1 ATGCATGCATGCATGCATGC >[prefix]_2.1 ATGCATGCATGCATGCATGC ...
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[prefix]_R2.fasta
>[prefix]_1.2 ATGCATGCATGCATGCATGC >[prefix]_2.2 ATGCATGCATGCATGCATGC ...