Describe the bug
In half of the pair-end reads in the FASTQ files, forward and reverse read sequences are identical. This is (correctly) not observed in the golden BAM file.
I encourage you to visit our most up-to-date repo for this code: https://github.com/ncsa/NEAT - We have identified and fixed this bug. I may pull those changes back to this repo.
Describe the bug In half of the pair-end reads in the FASTQ files, forward and reverse read sequences are identical. This is (correctly) not observed in the golden BAM file.
To Reproduce I created a github repo to describe the issue with a minimal reproducible example: https://github.com/Accio/NEAT-issue
Expected behavior Forward and reverse sequences in the FASTQ files should be distinct, and 100% mapped to the input genome.
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