Remove unused parameter
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@ -89,7 +89,7 @@ docker-run:
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--ref_annotation differential_expression/gencode.v22.annotation.chr20.gff \
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--direct_rna --minimap_index_opts '-k 15' \
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--ref_transcriptome differential_expression/ref_transcriptome.fasta \
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--transcriptome_assembly false --sample_sheet test_data/sample_sheet.csv"
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--sample_sheet test_data/sample_sheet.csv"
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NF_IGNORE_PROCESSES: >
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preprocess_reads,merge_transcriptomes,assemble_transcripts,decompress_annotation,decompress_ref,
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build_minimap_index,get_transcriptome,merge_gff_bundles,run_gffcompare,build_minimap_index,split_bam
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@ -103,7 +103,7 @@ docker-run:
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--ref_annotation differential_expression/gencode.v22.annotation.chr20.gff3 \
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--direct_rna --minimap_index_opts '-k 15' \
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--ref_transcriptome differential_expression/ref_transcriptome.fasta \
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--transcriptome_assembly false --sample_sheet test_data/sample_sheet.csv"
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--sample_sheet test_data/sample_sheet.csv"
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NF_IGNORE_PROCESSES: >
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preprocess_reads,merge_transcriptomes,assemble_transcripts,decompress_annotation,decompress_ref,
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build_minimap_index,get_transcriptome,merge_gff_bundles,run_gffcompare,build_minimap_index,split_bam
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@ -117,7 +117,7 @@ docker-run:
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--ref_genome differential_expression_ncbi/GRCh38.p14.NCBI_test.fna.gz \
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--ref_annotation differential_expression_ncbi/GRCh38.p14_NCBI_test.gtf.gz \
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--direct_rna --minimap_index_opts '-w 25' \
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--transcriptome_assembly false --sample_sheet test_data/sample_sheet.csv"
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--sample_sheet test_data/sample_sheet.csv"
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NF_IGNORE_PROCESSES: >
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preprocess_reads,merge_transcriptomes,assemble_transcripts,
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build_minimap_index,get_transcriptome,merge_gff_bundles,run_gffcompare,build_minimap_index,split_bam
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@ -241,7 +241,8 @@ nextflow run epi2me-labs/wf-transcriptomes \
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--de_analysis \
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--ref_genome differential_expression/hg38_chr20.fa \
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--ref_annotation differential_expression/gencode.v22.annotation.chr20.gtf \
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--direct_rna --minimap_index_opts \-k15
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--direct_rna --minimap_index_opts \
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-k15
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```
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You can also run the differential expression section of the workflow on its own by providing a reference transcriptome and setting the transcriptome assembly parameter to false.
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eg.
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@ -251,9 +252,9 @@ nextflow run epi2me-labs/wf-transcriptomes \
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--de_analysis \
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--ref_genome differential_expression/hg38_chr20.fa \
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--ref_annotation differential_expression/gencode.v22.annotation.chr20.gtf \
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--direct_rna --minimap_index_opts \-k15 \
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--ref_transcriptome differential_expression/ref_transcriptome.fasta \
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--transcriptome_assembly false
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--direct_rna --minimap_index_opts \
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-k15 \
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--ref_transcriptome differential_expression/ref_transcriptome.fasta
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```
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## Workflow outputs
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@ -151,7 +151,8 @@ nextflow run epi2me-labs/wf-transcriptomes \
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--de_analysis \
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--ref_genome differential_expression/hg38_chr20.fa \
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--ref_annotation differential_expression/gencode.v22.annotation.chr20.gtf \
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--direct_rna --minimap_index_opts \-k15
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--direct_rna --minimap_index_opts \
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-k15
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```
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You can also run the differential expression section of the workflow on its own by providing a reference transcriptome and setting the transcriptome assembly parameter to false.
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eg.
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@ -161,9 +162,9 @@ nextflow run epi2me-labs/wf-transcriptomes \
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--de_analysis \
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--ref_genome differential_expression/hg38_chr20.fa \
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--ref_annotation differential_expression/gencode.v22.annotation.chr20.gtf \
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--direct_rna --minimap_index_opts \-k15 \
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--ref_transcriptome differential_expression/ref_transcriptome.fasta \
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--transcriptome_assembly false
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--direct_rna --minimap_index_opts \
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-k15 \
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--ref_transcriptome differential_expression/ref_transcriptome.fasta
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```
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## Workflow outputs
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