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3.0 years ago
Baran
•
0
I'm sorry if this is a non-sense question but I am a rookie and although I searched about this I couldn't find any decent answer. I had the fastq files but they somehow became corrupted. I need to get Q20 Q30 scores for the fastq file but I only have bam files right now. So, I wonder if it is okay to get fastq files by converting bam files with the gatk SamToFastq convert function and then getting the Seqkit stat results?