Comments (1)
Hi Vitali,
The two files you mention (.rmdup.collapsed.bam
and .rmdup.normal.bam
) are intermediate files generated by the pipeline, prior to it filtering PCR duplicates. You should not be using these files without good reason. The BAM file you should be using is the ${Sample}.${Genome}.bam
file located in the root of your output directory (the same directory as the YAML file by default). That file will have been appropriately filtered for PCR duplicates in a unless you specifically turned it off.
See here for a detailed description of the output files of the pipeline:
https://paleomix.readthedocs.io/en/stable/bam_pipeline/filestructure.html
I would generally recommend merging PE reads, regardless of read quality. The only exception is if the DNA fragment size is much greater than about 300 bp (ie. twice your read length), since false positive merged reads will likely dominate in that case.
Best regards,
Mikkel
from paleomix.
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