using MitoZ in Docker, works well with my fastq.gz files but when I download from SRA, these reads fail. Looking at the output, the cleaned sequence file is empty. I assume there is some format issue between archived .fastq.gz files and what you get directly from Illumina sequencers. Any help would be greatly appreciated.
using MitoZ in Docker, works well with my fastq.gz files but when I download from SRA, these reads fail. Looking at the output, the cleaned sequence file is empty. I assume there is some format issue between archived .fastq.gz files and what you get directly from Illumina sequencers. Any help would be greatly appreciated.