workflows/well_fastqs_to_esets

Description

Map a list of FASTQ files (one for each well) to a reference genome and generate count matrices.
Sometimes counts from different FASTQ files need to be concatenated. This is done bases on the sample_id:
if the sample ID of the two plates are identical, the FASTQ files will we joined before mapping.

Type

nextflow_script

License

MIT

Contributors

Run this component

Run the following command to execute this component with Nextflow:

cat > params.yaml <<'EOM'  
umi_length: [ 10 ]  
star_output: "$id.$key.star_output._*"  
nrReadsNrGenesPerChrom: "$id.$key.nrReadsNrGenesPerChrom"  
star_qc_metrics: "$id.$key.star_qc_metrics"  
eset: "$id.$key.eset"  
f_data: "$id.$key.f_data"  
p_data: "$id.$key.p_data"  
html_report: "$id.$key.html_report"  
id: "run"  
publish_dir: "output/"  
EOM

nextflow run https://packages.viash-hub.com/vsh/htrnaseq.git \  
  -revision v0.15.0-rc.2 \  
  -main-script target/nextflow/workflows/well_fastqs_to_esets/main.nf \  
  -params-file params.yaml  

Input arguments

Name
Type & Properties
--input_r1
file
required
multiple
--input_r2
file
required
multiple
--barcodesFasta
file
required
--umi_length
integer
--genomeDir
file
required
--annotation
file
required
--sample_id
string
--run_params
file

Output arguments

Name
Type & Properties
--star_output
file
required
multiple
output
--nrReadsNrGenesPerChrom
file
required
output
--star_qc_metrics
file
required
output
--eset
file
required
output
--f_data
file
required
output
--p_data
file
required
output
--html_report
file
required
output

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Viash Hub is a platform developed by Data Intuitive, a Belgian-based bioinformatics company specializing in data workflow development and deployment.