Explore Workflows
View already parsed workflows here or click here to add your own
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bam to trimmed fastqs
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![]() Path: definitions/subworkflows/bam_to_trimmed_fastq.cwl Branch/Commit ID: 0b6e8fd8ead7644cf5398395b76af5cf4011686f |
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scatter-wf2.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/scatter-wf2.cwl Branch/Commit ID: 84939620c3eec1ab11369849c63237ebfa48da41 |
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Filter single sample sv vcf from paired read callers(Manta/Smoove)
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![]() Path: definitions/subworkflows/sv_paired_read_caller_filter.cwl Branch/Commit ID: 2decd55996b912feb48be5db1b052aa3274ee405 |
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Non-Coding Bacterial Genes
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![]() Path: bacterial_noncoding/wf_bacterial_noncoding.cwl Branch/Commit ID: f10de890d1d2271299931349fa8aea660acef4ee |
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pcr-bottleneck-coef.cwl
ChIP-seq - map - PCR Bottleneck Coefficients |
![]() Path: v1.0/map/pcr-bottleneck-coef.cwl Branch/Commit ID: 8d02684ae0ff27e641f3704686e3bc8b1979b854 |
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schemadef-wf.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/schemadef-wf.cwl Branch/Commit ID: 4df56e95e6fceab69e677b539f3532cbf5946197 |
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Exome QC workflow
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![]() Path: definitions/subworkflows/qc_exome_no_verify_bam.cwl Branch/Commit ID: b9e7392e72506cadd898a6ac4db330baf6535ab6 |
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count-lines7-wf.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/count-lines7-wf.cwl Branch/Commit ID: 84939620c3eec1ab11369849c63237ebfa48da41 |
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EMG pipeline's QIIME workflow
Step 1: Set environment PYTHONPATH, QIIME_ROOT, PATH Step 2: Run QIIME script pick_closed_reference_otus.py ${python} ${qiimeDir}/bin/pick_closed_reference_otus.py -i $1 -o $2 -r ${qiimeDir}/gg_13_8_otus/rep_set/97_otus.fasta -t ${qiimeDir}/gg_13_8_otus/taxonomy/97_otu_taxonomy.txt -p ${qiimeDir}/cr_otus_parameters.txt Step 3: Convert new biom format to old biom format (json) ${qiimeDir}/bin/biom convert -i ${resultDir}/cr_otus/otu_table.biom -o ${resultDir}/cr_otus/${infileBase}_otu_table_json.biom --table-type=\"OTU table\" --to-json Step 4: Convert new biom format to a classic OTU table. ${qiimeDir}/bin/biom convert -i ${resultDir}/cr_otus/otu_table.biom -o ${resultDir}/cr_otus/${infileBase}_otu_table.txt --to-tsv --header-key taxonomy --table-type \"OTU table\" Step 5: Create otu summary ${qiimeDir}/bin/biom summarize-table -i ${resultDir}/cr_otus/otu_table.biom -o ${resultDir}/cr_otus/${infileBase}_otu_table_summary.txt Step 6: Move one of the result files mv ${resultDir}/cr_otus/otu_table.biom ${resultDir}/cr_otus/${infileBase}_otu_table_hdf5.biom Step 7: Create a list of observations awk '{print $1}' ${resultDir}/cr_otus/${infileBase}_otu_table.txt | sed '/#/d' > ${resultDir}/cr_otus/${infileBase}_otu_observations.txt Step 8: Create a phylogenetic tree by pruning GreenGenes and keeping observed otus ${python} ${qiimeDir}/bin/filter_tree.py -i ${qiimeDir}/gg_13_8_otus/trees/97_otus.tree -t ${resultDir}/cr_otus/${infileBase}_otu_observations.txt -o ${resultDir}/cr_otus/${infileBase}_pruned.tree |
![]() Path: workflows/qiime-workflow.cwl Branch/Commit ID: 316831663e84623eb0e3a260af252fef441924d4 |
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Run tRNAScan
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![]() Path: bacterial_trna/wf_trnascan.cwl Branch/Commit ID: f10de890d1d2271299931349fa8aea660acef4ee |