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Update analysis outputs in SmartSeq2 Adapter WDL (#72)
* Update SS2 adapter analysis outputs * Update docker tag
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adapter_pipelines/ss2_single_sample/adapter.wdl

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Original file line numberDiff line numberDiff line change
@@ -83,7 +83,7 @@ workflow AdapterSmartSeq2SingleCell{
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Int max_cromwell_retries = 0
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Boolean add_md5s = false
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String pipeline_tools_version = "v0.29.0"
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String pipeline_tools_version = "v0.30.0"
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call GetInputs as prep {
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input:
@@ -177,39 +177,18 @@ workflow AdapterSmartSeq2SingleCell{
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"value": stranded
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}
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],
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outputs = [
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outputs = flatten([[
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analysis.aligned_bam,
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analysis.alignment_summary_metrics,
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analysis.bait_bias_detail_metrics,
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analysis.bait_bias_summary_metrics,
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analysis.base_call_dist_metrics,
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analysis.base_call_pdf,
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analysis.dedup_metrics,
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analysis.error_summary_metrics,
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analysis.gc_bias_detail_metrics,
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analysis.gc_bias_dist_pdf,
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analysis.gc_bias_summary_metrics,
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analysis.insert_size_hist,
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analysis.bam_index,
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analysis.insert_size_metrics,
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analysis.hisat2_log_file,
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analysis.hisat2_met_file,
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analysis.pre_adapter_details_metrics,
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analysis.quality_by_cycle_metrics,
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analysis.quality_by_cycle_pdf,
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analysis.quality_distribution_dist_pdf,
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analysis.quality_distribution_metrics,
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analysis.rna_coverage,
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analysis.quality_by_cycle_metrics,
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analysis.bait_bias_summary_metrics,
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analysis.rna_metrics,
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analysis.aligned_transcriptome_bam,
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analysis.hisat2_transcriptome_log_file,
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analysis.hisat2_transcriptome_met_file,
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analysis.rsem_cnt_log,
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analysis.rsem_gene_results,
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analysis.rsem_isoform_results,
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analysis.rsem_model_log,
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analysis.rsem_theta_log,
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analysis.rsem_time_log
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],
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analysis.rsem_isoform_results
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], analysis.group_results]),
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format_map = format_map,
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submit_url = submit_url,
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cromwell_url = cromwell_url,

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