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Added simplified version of SRWholeGenome.
- Added `SRWholeGenome_Simplified.wdl` which uses a simplified version of the HaplotypeCaller workflow to run faster. This was accomplished by removing the scatter by interval. This workflow will not scatter by interval when performing variant calling. This is OK for small genomes / organisms. - Added `HaplotypeCaller_Simplified.wdl` which performs germline variant calling on an input bam file without any scattering.
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