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.
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 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 |
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 |