Page Index - genome/analysis-workflows GitHub Wiki
552 page(s) in this GitHub Wiki:
- Home
- Overview
- Featured Pipelines
- Whole Genome Clinical Assay
- Inputs
- Table of Contents
- Tools
- Subworkflows
- Pipelines
- Questions
- Alignment
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- Bisulfite workflow
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- Creating RNAseq annotation files from Ensembl
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- DNA Alignment
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- Frequently Asked Questions (FAQ)
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- Fusions
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- Gathering input files
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- Germline SNVs and small Indels
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- Legacy Setup Instructions
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- Legacy SNVs_and_SmallIndels
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- pipelines
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- pipelines_alignment_exome.cwl
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- pipelines_alignment_exome_nonhuman.cwl
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- pipelines_alignment_umi_duplex.cwl
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- pipelines_alignment_umi_molecular.cwl
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- pipelines_alignment_wgs.cwl
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- pipelines_alignment_wgs_nonhuman.cwl
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- pipelines_aml_trio_cle.cwl
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- pipelines_aml_trio_cle_gathered.cwl
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- pipelines_bisulfite.cwl
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- pipelines_chipseq.cwl
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- pipelines_chipseq_alignment_nonhuman.cwl
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- pipelines_detect_variants.cwl
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- pipelines_detect_variants_nonhuman.cwl
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- pipelines_detect_variants_wgs.cwl
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- pipelines_detect_variants_wgs_nonhuman.cwl
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- pipelines_downsample_and_recall.cwl
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- pipelines_gathered_downsample_and_recall.cwl
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- pipelines_germline_exome.cwl
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- pipelines_germline_exome_gvcf.cwl
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- pipelines_germline_exome_hla_typing.cwl
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- pipelines_germline_wgs.cwl
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- pipelines_germline_wgs_gvcf.cwl
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- pipelines_immuno.cwl
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- pipelines_rnaseq.cwl
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- pipelines_rnaseq_star_fusion.cwl
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- pipelines_rnaseq_star_fusion_with_xenosplit.cwl
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- pipelines_somatic_exome.cwl
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- pipelines_somatic_exome_cle.cwl
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- pipelines_somatic_exome_cle_gathered.cwl
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- pipelines_somatic_exome_gathered.cwl
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- pipelines_somatic_exome_nonhuman.cwl
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- pipelines_somatic_wgs.cwl
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- pipelines_somatic_wgs_nonhuman.cwl
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- pipelines_tumor_only_detect_variants.cwl
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- pipelines_tumor_only_exome.cwl
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- pipelines_tumor_only_wgs.cwl
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- README
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- RnaSeq
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- Single Sample SVs
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- subworkflows
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- subworkflows_align.cwl
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- subworkflows_align_sort_markdup.cwl
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- subworkflows_bam_readcount.cwl
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- subworkflows_bam_to_trimmed_fastq_and_biscuit_alignments.cwl
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- subworkflows_bgzip_and_index.cwl
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- subworkflows_bisulfite_qc.cwl
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- subworkflows_cellranger_mkfastq_and_count.cwl
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- subworkflows_cnvkit_single_sample.cwl
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- subworkflows_cram_to_bam_and_index.cwl
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- subworkflows_cram_to_cnvkit.cwl
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- subworkflows_docm_cle.cwl
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- subworkflows_docm_germline.cwl
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- subworkflows_duplex_alignment.cwl
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- subworkflows_filter_vcf.cwl
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- subworkflows_filter_vcf_nonhuman.cwl
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- subworkflows_fp_filter.cwl
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- subworkflows_gatk_haplotypecaller_iterator.cwl
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- subworkflows_generate_fda_metrics.cwl
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- subworkflows_germline_detect_variants.cwl
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- subworkflows_germline_filter_vcf.cwl
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- subworkflows_hs_metrics.cwl
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- subworkflows_joint_genotype.cwl
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- subworkflows_merge_svs.cwl
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- subworkflows_molecular_alignment.cwl
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- subworkflows_molecular_qc.cwl
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- subworkflows_mutect.cwl
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- subworkflows_phase_vcf.cwl
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- subworkflows_pindel.cwl
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- subworkflows_pindel_cat.cwl
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- subworkflows_pindel_region.cwl
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- subworkflows_pvacseq.cwl
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- subworkflows_qc_exome.cwl
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- subworkflows_qc_exome_no_verify_bam.cwl
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- subworkflows_qc_wgs.cwl
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- subworkflows_qc_wgs_nonhuman.cwl
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- subworkflows_sequence_align_and_tag_adapter.cwl
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- subworkflows_sequence_to_bqsr.cwl
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- subworkflows_sequence_to_bqsr_nonhuman.cwl
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- subworkflows_sequence_to_trimmed_fastq.cwl
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- subworkflows_sequence_to_trimmed_fastq_and_hisat_alignments.cwl
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- subworkflows_single_cell_rnaseq.cwl
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- subworkflows_single_sample_sv_callers.cwl
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- subworkflows_strelka_and_post_processing.cwl
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- subworkflows_strelka_process_vcf.cwl
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- subworkflows_sv_depth_caller_filter.cwl
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- subworkflows_sv_paired_read_caller_filter.cwl
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- subworkflows_umi_alignment.cwl
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- subworkflows_varscan.cwl
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- subworkflows_varscan_germline.cwl
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- subworkflows_varscan_pre_and_post_processing.cwl
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- subworkflows_vcf_eval_cle_gold.cwl
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- subworkflows_vcf_eval_concordance.cwl
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- subworkflows_vcf_readcount_annotator.cwl
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- tools
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- tools_add_strelka_gt.cwl
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- tools_add_string_at_line.cwl
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- tools_add_string_at_line_bgzipped.cwl
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- tools_add_vep_fields_to_table.cwl
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- tools_agfusion.cwl
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- tools_align_and_tag.cwl
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- tools_aligned_seq_fda_stats.cwl
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- tools_annotsv.cwl
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- tools_annotsv_filter.cwl
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- tools_apply_bqsr.cwl
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- tools_bam_readcount.cwl
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- tools_bam_to_bigwig.cwl
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- tools_bam_to_cram.cwl
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- tools_bam_to_fastq.cwl
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- tools_bam_to_sam.cwl
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- tools_bcftools_merge.cwl
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- tools_bedgraph_to_bigwig.cwl
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- tools_bedtools_intersect.cwl
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- tools_bgzip.cwl
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- tools_biscuit_align.cwl
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- tools_biscuit_markdup.cwl
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- tools_biscuit_pileup.cwl
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- tools_bisulfite_qc_conversion.cwl
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- tools_bisulfite_qc_coverage_stats.cwl
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- tools_bisulfite_qc_cpg_retention_distribution.cwl
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- tools_bisulfite_qc_mapping_summary.cwl
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- tools_bisulfite_vcf2bed.cwl
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- tools_bqsr.cwl
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- tools_call_duplex_consensus.cwl
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- tools_call_molecular_consensus.cwl
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- tools_cat_all.cwl
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- tools_cat_out.cwl
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- tools_cellmatch_lineage.cwl
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- tools_cellranger_atac_count.cwl
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- tools_cellranger_count.cwl
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- tools_cellranger_feature_barcoding.cwl
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- tools_cellranger_mkfastq.cwl
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- tools_cellranger_vdj.cwl
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- tools_cle_aml_trio_report_alignment_stat.cwl
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- tools_cle_aml_trio_report_coverage_stat.cwl
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- tools_cle_aml_trio_report_full_variants.cwl
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- tools_clip_overlap.cwl
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- tools_cnvkit_batch.cwl
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- tools_cnvkit_vcf_export.cwl
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- tools_cnvnator.cwl
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- tools_collect_alignment_summary_metrics.cwl
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- tools_collect_gc_bias_metrics.cwl
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- tools_collect_hs_metrics.cwl
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- tools_collect_insert_size_metrics.cwl
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- tools_collect_wgs_metrics.cwl
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- tools_combine_gvcfs.cwl
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- tools_combine_variants.cwl
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- tools_combine_variants_concordance.cwl
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- tools_combine_variants_wgs.cwl
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- tools_concordance.cwl
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- tools_cram_to_bam.cwl
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- tools_docm_add_variants.cwl
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- tools_docm_gatk_haplotype_caller.cwl
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- tools_downsample.cwl
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- tools_duphold.cwl
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- tools_duplex_seq_metrics.cwl
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- tools_eval_cle_gold.cwl
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- tools_eval_vaf_report.cwl
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- tools_extract_hla_alleles.cwl
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- tools_extract_umis.cwl
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- tools_fastq_to_bam.cwl
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- tools_fastqc.cwl
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- tools_filter_consensus.cwl
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- tools_filter_known_variants.cwl
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- tools_filter_sv_vcf_blocklist_bedpe.cwl
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- tools_filter_sv_vcf_depth.cwl
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- tools_filter_sv_vcf_read_support.cwl
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- tools_filter_sv_vcf_size.cwl
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- tools_filter_vcf_cle.cwl
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- tools_filter_vcf_coding_variant.cwl
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- tools_filter_vcf_custom_allele_freq.cwl
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- tools_filter_vcf_depth.cwl
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- tools_filter_vcf_docm.cwl
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- tools_filter_vcf_mapq0.cwl
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- tools_filter_vcf_somatic_llr.cwl
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- tools_fix_vcf_header.cwl
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- tools_fp_filter.cwl
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- tools_gather_to_sub_directory.cwl
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- tools_gatherer.cwl
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- tools_gatk_genotypegvcfs.cwl
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- tools_gatk_haplotype_caller.cwl
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- tools_generate_fda_tables.cwl
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- tools_generate_qc_metrics.cwl
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- tools_germline_combine_variants.cwl
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- tools_grolar.cwl
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- tools_group_reads.cwl
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- tools_hisat2_align.cwl
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- tools_hla_consensus.cwl
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- tools_homer_tag_directory.cwl
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- tools_index_bam.cwl
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- tools_index_cram.cwl
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- tools_index_vcf.cwl
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- tools_intersect_known_variants.cwl
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- tools_interval_list_expand.cwl
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- tools_intervals_to_bed.cwl
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- tools_kallisto.cwl
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- tools_kmer_size_from_index.cwl
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- tools_manta_somatic.cwl
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- tools_mark_duplicates_and_sort.cwl
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- tools_mark_illumina_adapters.cwl
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- tools_md5sum.cwl
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- tools_merge_bams.cwl
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- tools_merge_bams_samtools.cwl
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- tools_merge_vcf.cwl
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- tools_mutect.cwl
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- tools_name_sort.cwl
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- tools_normalize_variants.cwl
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- tools_optitype_dna.cwl
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- tools_picard_merge_vcfs.cwl
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- tools_pindel.cwl
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- tools_pindel2vcf.cwl
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- tools_pindel_somatic_filter.cwl
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- tools_pizzly.cwl
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- tools_pvacbind.cwl
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- tools_pvacfuse.cwl
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- tools_pvacseq.cwl
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- tools_pvacseq_combine_variants.cwl
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- tools_pvacvector.cwl
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- tools_read_backed_phasing.cwl
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- tools_realign.cwl
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- tools_remove_end_tags.cwl
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- tools_rename.cwl
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- tools_rename_for_staging.cwl
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- tools_replace_vcf_sample_name.cwl
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- tools_samtools_flagstat.cwl
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- tools_samtools_sort.cwl
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- tools_select_variants.cwl
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- tools_sequence_align_and_tag.cwl
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- tools_sequence_to_bam.cwl
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- tools_sequence_to_fastq.cwl
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- tools_set_filter_status.cwl
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- tools_single_sample_docm_filter.cwl
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- tools_smoove.cwl
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- tools_somatic_concordance_graph.cwl
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- tools_sompy.cwl
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- tools_sort_vcf.cwl
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- tools_split_interval_list.cwl
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- tools_split_interval_list_to_bed.cwl
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- tools_staged_rename.cwl
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- tools_star_align_fusion.cwl
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- tools_star_fusion_detect.cwl
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- tools_strandedness_check.cwl
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- tools_strelka.cwl
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- tools_stringtie.cwl
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- tools_survivor.cwl
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- tools_transcript_to_gene.cwl
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- tools_trim_fastq.cwl
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- tools_umi_align.cwl
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- tools_unaligned_seq_fda_stats.cwl
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- tools_variants_to_table.cwl
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- tools_varscan_germline.cwl
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- tools_varscan_process_somatic.cwl
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- tools_varscan_somatic.cwl
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- tools_vcf_expression_annotator.cwl
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- tools_vcf_readcount_annotator.cwl
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- tools_vcf_sanitize.cwl
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- tools_vep.cwl
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- tools_verify_bam_id.cwl
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- tools_vt_decompose.cwl
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- tools_xenosplit.cwl
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- Whole Genome Sequencing Clinical Assay
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