Explore Workflows
View already parsed workflows here or click here to add your own
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salmon-workflow.cwl
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![]() Path: salmon-workflow.cwl Branch/Commit ID: 9772782d041c4d0a180fc89d55c83c31b24bb6af |
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pass-unconnected.cwl
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![]() Path: v1.0/v1.0/pass-unconnected.cwl Branch/Commit ID: ca8e6661b5cab1f017e5bc4024650722dae4d50b |
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Unaligned BAM to BQSR and VCF
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![]() Path: definitions/subworkflows/bam_to_bqsr_no_dup_marking.cwl Branch/Commit ID: c625e05eefb1754353c1bdfa46c01dc61e6233dd |
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Add snv and indel bam-readcount files to a vcf
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![]() Path: definitions/subworkflows/vcf_readcount_annotator.cwl Branch/Commit ID: 3a287b7cb6162cdea79865235d224fea45963d87 |
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atm-plev-n2n.cwl
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![]() Path: scripts/cwl_workflows/atm-unified/atm-plev-n2n.cwl Branch/Commit ID: 330559dfb86d112fd2d3b0ef05a630622766f5ec |
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gatk4W.cwl
Author: AMBARISH KUMAR er.ambarish@gmail.com & ambari73_sit@jnu.ac.in This is a proposed standard operating procedure for genomic variant detection using GATK4. It is hoped to be effective and useful for getting SARS-CoV-2 genome variants. It uses Illumina RNASEQ reads and genome sequence. |
![]() Path: gatk4W.cwl Branch/Commit ID: dccb12c85526c878ce3a489f9502350d187955a5 |
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downsample unaligned BAM and align
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![]() Path: definitions/subworkflows/downsampled_alignment.cwl Branch/Commit ID: 038cb3617a1966a1057386adcde97ce55d9e1139 |
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bam_readcount workflow
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![]() Path: definitions/subworkflows/bam_readcount.cwl Branch/Commit ID: 038cb3617a1966a1057386adcde97ce55d9e1139 |
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EMG assembly for paired end Illumina
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![]() Path: workflows/emg-assembly.cwl Branch/Commit ID: 2104dc36c775de93de3fef77e7f82a19da76b6e3 |
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etl.cwl
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![]() Path: workflows/fastq_readgroup_stats/etl.cwl Branch/Commit ID: 1046947f8d2923e6563b3aceac9e435554c5bea1 |