Resolve CW-2700 "Demo not working"
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README.md
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README.md
@ -140,9 +140,9 @@ nextflow run epi2me-labs/wf-transcriptomes \
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**Example workflow for denovo transcript assembly**
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```
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OUTPUT=~/output
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nextflow run . --fastq test_data/fastq \
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--denovo \
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--ref_genome test_data/SIRV_150601a.fasta \
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nextflow run epi2me-labs/wf-transcriptomes \
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--fastq test_data/fastq \
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--transcriptome_source denovo \
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--out_dir ${OUTPUT} \
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-w ${OUTPUT}/workspace \
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--sample sample_id
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@ -235,14 +235,15 @@ Here is an example cmd to run the workflow. First you will need to download the
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eg.
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```
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wget -O differential_expression.tar.gz https://ont-exd-int-s3-euwst1-epi2me-labs.s3.amazonaws.com/wf-isoforms/differential_expression.tar.gz && tar -xzvf differential_expression.tar.gz
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OUTPUT=~/output;
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nextflow run epi2me-labs/wf-transcriptomes \
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--fastq differential_expression/differential_expression_fastq \
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--transcriptome-source precomputed \
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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 --minimap2_index_opts \
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-k15
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--ref_annotation differential_expression/gencode.v22.annotation.chr20.gff \
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--direct_rna --minimap2_index_opts '-k 15' \
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--ref_transcriptome differential_expression/ref_transcriptome.fasta \
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--sample_sheet test_data/sample_sheet.csv
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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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@ -252,9 +253,9 @@ 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 --minimap2_index_opts \
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-k15 \
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--ref_transcriptome differential_expression/ref_transcriptome.fasta
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--direct_rna --minimap2_index_opts '-k 15' \
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--ref_transcriptome differential_expression/ref_transcriptome.fasta \
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--sample_sheet test_data/sample_sheet.csv
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```
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## Workflow outputs
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@ -50,9 +50,9 @@ nextflow run epi2me-labs/wf-transcriptomes \
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**Example workflow for denovo transcript assembly**
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```
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OUTPUT=~/output
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nextflow run . --fastq test_data/fastq \
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--denovo \
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--ref_genome test_data/SIRV_150601a.fasta \
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nextflow run epi2me-labs/wf-transcriptomes \
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--fastq test_data/fastq \
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--transcriptome_source denovo \
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--out_dir ${OUTPUT} \
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-w ${OUTPUT}/workspace \
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--sample sample_id
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@ -145,14 +145,15 @@ Here is an example cmd to run the workflow. First you will need to download the
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eg.
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```
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wget -O differential_expression.tar.gz https://ont-exd-int-s3-euwst1-epi2me-labs.s3.amazonaws.com/wf-isoforms/differential_expression.tar.gz && tar -xzvf differential_expression.tar.gz
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OUTPUT=~/output;
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nextflow run epi2me-labs/wf-transcriptomes \
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--fastq differential_expression/differential_expression_fastq \
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--transcriptome-source precomputed \
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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 --minimap2_index_opts \
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-k15
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--ref_annotation differential_expression/gencode.v22.annotation.chr20.gff \
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--direct_rna --minimap2_index_opts '-k 15' \
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--ref_transcriptome differential_expression/ref_transcriptome.fasta \
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--sample_sheet test_data/sample_sheet.csv
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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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@ -162,9 +163,9 @@ 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 --minimap2_index_opts \
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-k15 \
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--ref_transcriptome differential_expression/ref_transcriptome.fasta
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--direct_rna --minimap2_index_opts '-k 15' \
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--ref_transcriptome differential_expression/ref_transcriptome.fasta \
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--sample_sheet test_data/sample_sheet.csv
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```
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## Workflow outputs
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