Workflow: Whole Exome Sequencing
Whole Exome Sequence analysis using GATK best practices - Germline SNP & Indel Discovery
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 - Default Values
 - Nested Workflows
 - Tools
 - Inputs/Outputs
 
                This workflow is Open Source and may be reused according to the terms of:
                
                    MIT License
                
                
            
            Note that the tools invoked by the workflow may have separate licenses.
            Inputs
| ID | Type | Title | Doc | 
|---|---|---|---|
| GATKJar | File | ||
| library | String | ||
| threads | Integer (Optional) | ||
| platform | String | ||
| intervals | File[] (Optional) | ||
| knownSites | File[] | ||
| read_pairs | https://w3id.org/cwl/view/git/e2dc95d4f12210359360d814382e7201d836dfcf/packed/exomeseq.cwl#bespin-types.yml/NamedFASTQFilePairType[] | ||
| study_type | https://w3id.org/cwl/view/git/e2dc95d4f12210359360d814382e7201d836dfcf/packed/exomeseq.cwl#bespin-types.yml/ExomeseqStudyType | ||
| resource_dbsnp | File | ||
| interval_padding | Integer (Optional) | ||
| reference_genome | File | ||
| snp_resource_1kg | File | ||
| primary_intervals | File[] (Optional) | ||
| snp_resource_omni | File | ||
| snp_resource_hapmap | File | ||
| indel_resource_mills | File | 
Steps
| ID | Runs | Label | Doc | 
|---|---|---|---|
| preprocessing | 
                                 
                                    exomeseq.cwl#exomeseq-01-preprocessing.cwl
                                    
                                    (Workflow)
                                 
                                
                             | 
                            ||
| variant_discovery | |||
| organize_directories | |||
| prepare_reference_data | 
Outputs
| ID | Type | Label | Doc | 
|---|---|---|---|
| bams_final_dir | Directory | 
                                     BAM files containing assembled haplotypes and locally realigned reads  | 
                            |
| hs_metrics_dir | Directory | ||
| raw_variants_dir | Directory | ||
| trim_reports_dir | Directory | ||
| fastqc_reports_dir | Directory | ||
| joint_raw_variants | File | 
                                     GVCF file from joint genotyping calling  | 
                            |
| bams_markduplicates_dir | Directory | 
                                     BAM and bai files from markduplicates  | 
                            |
| filtered_recalibrated_variants | File | 
                                     The output filtered and recalibrated VCF file in which each variant is annotated with its VQSLOD value  | 
                            
      Permalink:
        
https://w3id.org/cwl/view/git/e2dc95d4f12210359360d814382e7201d836dfcf/packed/exomeseq.cwl?part=main
      
    