Open morglind opened 6 years ago
Totally! QC should definitely catch issues like this.
Commit 19f4edea771553196f227475ea03c54d48e46160 should "fix" this.
It's a heuristic, as it just assumes that the forward and reverse strand files should be relatively the same size. A full check would be relatively time consuming. Also, I would think that all successfully bcl2fastq (assuming illumina only) demultiplexed fastq paired-end files should have the same number of forward and reverse strand reads.
Although, maybe we should add an option in the cli to perform this task.
Can we add a QC step that verifies there is the same number of forward and reverse reads?