* add interleaved fastq option to sam2fastq
* add optional adapter trimming path
* add "skip_revert" option to skip reverting the bams (sometimes useful -- hidden parameter)
* add a walker that reads in one bam file and outputs N bam files, one for each read group in the original bam. This is a very important step in any BAM reprocessing pipeline.
I am using this new pipeline to process the CEU and YRI PCR Free WGS
trios.
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