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8.4 years ago
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I am attempting to error correct my illumina short reads using QuoRum error corrector (part of Masurca genome assembler; but I have installed only QuoRum and not Masurca). The output is a fasta file. I am unable to find the option to get the output file in fastQ format instead of fasta.
Can anybody who has experience with quorum, let me know the option to get output as fastq file ?