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Hello, I don't know why your software doesn't seem to work, and it doesn't generate output files after running, but my original fastq file becomes empty. Hope to get your answer, thank you.
(gcc) [guest@login BRCA]$ intent SRR7192118_1.fastq.gz SRR7192118_2.fastq.gz output
| Total | OK | Poor W1 | Too Short | Corrected | Bad Barcode |
|---|
Complete. Job summary:
Reads: 0
OK: 0
Poor W1 alignment: 0
Barcode or UMI too short: 0
Barcode succesfully corrected: 0
Barcode not recognized: 0
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