bases2fastq
demultiplex
fastq
demux
Element Biosciences
Description
Bases2Fastq demultiplexes sequencing data generated by Element Biosciences instruments and converts base calls into FASTQ files.
Input
Name | Type & Properties | Description |
|---|---|---|
--analysis_directory | file required | Location of analysis directory |
--run_manifest -r | file | Location of run manifest to use instead of default RunManifest.csv found in analysis directory |
Output
Name | Type & Properties | Description |
|---|---|---|
--output_directory -o | file required output | Location to save output fastqs |
--report | file output | Output location for the HTML report |
--logs | file output | Directory containing log files |
Arguments
Name | Type & Properties | Description |
|---|---|---|
--chemistry_version | string | Run parameters override, chemistry version. |
--demux_only -d | boolean_true | Generate demux files and indexing stats without generating FASTQ |
--detect_adapters | boolean_true | Detect adapters sequences, overriding any sequences present in run manifest. |
--error_on_missing | boolean_true | Terminate execution for a missing file (by default, missing files are skipped and execution continues). Also set by --strict. |
--exclude_tile -e | string multiple | Regex matching tile names to exclude. This flag can be specified multiple times. (e.g. L1.*C0[23]S.) |
--filter_mask | string | Run parameters override, custom pass filter mask. |
--flowcell_id | string | Run parameters override, flowcell ID. |
--force_index_orientation | boolean_true | Do not attempt to find orientation for I1/I2 reads (reverse complement). Use orientation given in run manifest. |
--group_fastq | boolean_true | Group all FASTQ/stats/metrics for a project are in the project folder. |
--i1_cycles | integer | Run parameters override, I1 cycles. |
--i2_cycles | integer | Run parameters override, I2 cycles |
--include_tile -i | string multiple | Regex matching tile names to include. This flag can be specified multiple times. (e.g. L1.*C0[23]S.) |
--kit_configuration | string | Run parameters override, kit configuration. |
--legacy_fastq | boolean_true | Legacy naming for FASTQ files (e.g. SampleName_S1_L001_R1_001.fastq.gz) |
--log_level -l | string | Severity level for logging. |
--no_error_on_invalid | boolean_true | Skip invalid files and continue execution. Overridden by --strict options |
--no_projects | boolean_true | Disable project directories |
--num_unassigned | integer | Max Number of unassigned sequences to report. |
--preparation_workflow | string | Run parameters override, preparation workflow. |
--qc_only | boolean_true | Quickly generate run stats for single tile without generating FASTQ. Use --include_tile/--exclude_tile to define custom tile set. |
--r1_cycles | integer | Run parameters override, R1 cycles. |
--r2_cycles | integer | Run parameters override, R2 cycles. |
--split_lanes | boolean_true | Split FASTQ files by lane. |
--strict | boolean_true | In strict mode any invalid or missing input file will terminate execution (overrides no_error_on_invalid and sets --error_on_missing) |
Run this component
Run the following command to execute this component with Nextflow:
cat > params.yaml <<'EOM'
output_directory: "$id.$key.output_directory.fastq_dir"
report: "$id.$key.report"
logs: "$id.$key.logs.logs_dir"
id: "run"
publish_dir: "output/"
EOM
nextflow run https://packages.viash-hub.com/vsh/biobox.git \
-revision v0.3.0 \
-main-script target/nextflow/bases2fastq/main.nf \
-params-file params.yaml Relationships
Used by
1 relationships
Current component
bases2fastqbiobox v0.3.0
Uses
0 relationships
No component dependencies found.