nf-core/airrflow
B-cell and T-cell Adaptive Immune Receptor Repertoire (AIRR) sequencing analysis pipeline using the Immcantation framework
3.2.0). The latest
stable release is
4.1.0
.
Define where the pipeline should find input data and save output data.
Path to comma-separated file containing information about the samples in the experiment.
string^\S+\.tsv$You will need to create a design file with information about the samples in your experiment before running the pipeline. Use this parameter to specify its location. It has to be a comma-separated file with 3 columns, and a header row. See usage docs.
Specify the processing mode for the pipeline. Available options are "fastq" and "assembled".
stringThe output directory where the results will be saved. You have to use absolute paths to storage on Cloud infrastructure.
stringEmail address for completion summary.
string^([a-zA-Z0-9_\-\.]+)@([a-zA-Z0-9_\-\.]+)\.([a-zA-Z]{2,5})$Set this parameter to your e-mail address to get a summary e-mail with details of the run sent to you when the workflow exits. If set in your user config file (~/.nextflow/config) then you don't need to specify this on the command line for every run.
Path to MiAIRR-BioSample mapping
stringairrflow/assets/reveal/mapping_MiAIRR_BioSample_v1.3.1.tsvExperimental protocol used to generate the data
Protocol used for the V(D)J amplicon sequencing library generation.
stringAvailable protocols are:
specific_pcr_umi: RT-PCR using transcript-specific primers containing UMIs.specific_pcr: RT-PCR using transcript-specific primers.dt_5p_race_umi: 5’-RACE PCR using oligo-dT primers and template switch primers containing UMI.dt_5p_race: 5’-RACE PCR (i.e. RT is followed by a template switch (TS) step) using oligo-dT primers.
Path to fasta file containing the linker sequence, if no V-region primers were used but a linker sequence is present (e.g. 5' RACE SMARTer TAKARA protocol).
stringDefine the primer region start and how to deal with the primer alignment.
Path to a fasta file containinc the V-region primer sequences.
stringPath to a fasta file containing the C-region primer sequences.
stringStart position of V region primers (without counting the UMI barcode).
integerStart position of C region primers (without counting the UMI barcode).
integerIndicate if C region primers are in the R1 or R2 reads.
stringSpecify to match the tail-end of the sequence against the reverse complement of the primers. This also reverses the behavior of the --start argument, such that start position is relative to the tail-end of the sequence. (default: False)Maximum scoring error for the Presto MaxPrimer process for the C and/or V region primers identification.
booleanDefine how UMI barcodes should be treated.
Indicate if UMI indices are recorded in the R1 (default) or R1 fastq file.
stringThe pipeline requires UMI barcodes for identifying unique transcripts. These barcodes are typically read from an index file but sometimes can be provided merged with the start of the R1 or R2 reads. If provided in an additional index file, set the --index_file parameter, if provided merged with the R1 or R2 reads, set the --umi_position parameter to R1 or R2, respectively.
UMI barcode length in nucleotides. Set to 0 if no UMIs present.
integer-1UMI barcode start position in the index read.
integerIndicate if UMI indices are recorded in a separate index file.
booleanSet to true if UMI barcodes are to be read from a separate Illumina index fastq file. If Illumina indices and UMI barcodes are already integrated into the R1 reads, leave the default --index_file false.
The pipeline requires UMI barcodes for identifying unique transcripts. These barcodes are typically read from an index file but sometimes can be provided merged with the start of the R1 or R2 reads. If provided in an additional index file, set the --index_file parameter, if provided merged with the R1 or R2 reads, set the --umi_position parameter.
Options for adapter trimming and read clipping
Whether to trim adapters in fastq reads with fastp.
booleantrueBy default adapters will be auto-detected, but adapter sequences can also be provided in a fasta file with the --adapter_fasta option.
Fasta file with adapter sequences to be trimmed.
stringNoneNumber of bases to clip 5' in R1 reads.
integerNumber of bases to clip 5' in R2 reads.
integerNumber of bases to clip 3' in R1 reads.
integerNumber of bases to clip 3' in R2 reads.
integerTrim adapters specific for Nextseq sequencing
booleanOption to save trimmed reads.
booleanOptions for the pRESTO sequence assembly processes
Quality threshold for pRESTO FilterSeq sequence filtering.
integer20Maximum primer scoring error in the pRESTO MaskPrimer step for the C and/or V region primers identification.
number0.2Maximum error for building the primer consensus in the pRESTO Buildconsensus step.
number0.6Masking mode for the pRESTO MaskPrimer step. Available: cut, mask, trim, tag.
stringThe primer masking modes will perform the following actions:
cut: remove both the primer region and the preceding sequence.mask: replace the primer region with Ns and remove the preceding sequence.trim: remove the region preceding the primer, but leave the primer region intact.tag: leave the input sequence unmodified.
Maximum error for building the sequence consensus in the pRESTO BuildConsensus step.
number0.1Maximum gap for building the sequence consensus in the pRESTO BuildConsensus step.
number0.5Cluster sequences by similarity regardless of any annotation with pRESTO ClusterSets and annotate the cluster ID additionally to the UMI barcode.
booleantrueOptions for the VDJ annotation processes.
Whether to reassign genes if the input file is an AIRR formatted tabulated file.
booleantrueSubset to productive sequences.
booleantrueSave databases so you can use the cache in future runs.
booleanPath to the cached IMGT database.
stringBy default, we provide a pre-downloaded version of the IMGT database. It is also possible to provide a custom IMGT reference database. To fetch a fresh version of IMGT, set the --fetch_imgt parameter instead.
Path to the cached igblast database.
stringBy default, we provide a pre-downloaded version of the IMGT database. It is also possible to provide a custom IMGT reference database. To fetch a fresh version of IMGT, set the --fetch_imgt parameter instead.
Set this flag to fetch the IMGT reference data at runtime.
booleanOptions for bulk sequence filtering after VDJ assignment.
Name of the field used to collapse duplicated sequences.
stringsample_idWhether to run the process to detect contamination.
booleanWhether to apply the chimera removal filter.
booleanDefine how the B-cell clonal trees should be calculated.
Set the clustering threshold Hamming distance value. Default: 'auto'
string,numberautoSkip clonal lineage analysis and lineage tree plotting.
booleanName of the field used to group data files to identify clones.
stringsubject_idName of the field used to identify external groups used to identify a clonal threshold.
stringsubject_idPath to IgPhyml executable.
string/usr/local/share/igphyml/src/igphymlName of the field used to determine if a sample is single cell sequencing or not.
stringsingle_cellSkip report of EnchantR DefineClones for all samples together.
booleanSkip report of EnchantR FindThreshold for all samples together.
booleanCustom report Rmarkdown file.
string${projectDir}/assets/repertoire_comparison.RmdCustom report style file in css format.
string${projectDir}/assets/nf-core_style.cssCustom logo for the report.
string${projectDir}/assets/nf-core-airrflow_logo_light.pngCustom logo for the EnchantR reports.
string${projectDir}/assets/nf-core-airrflow_logo_reports.pngSkip repertoire analysis and report generation.
booleanSkip multiqc report.
booleanOptions for the reference genome indices used to align reads.
Directory / URL base for iGenomes references.
strings3://ngi-igenomes/igenomesDo not load the iGenomes reference config.
booleantrueDo not load igenomes.config when running the pipeline. You may choose this option if you observe clashes between custom parameters and those supplied in igenomes.config.
Parameters used to describe centralised config profiles. These should not be edited.
Git commit id for Institutional configs.
stringmasterBase directory for Institutional configs.
stringhttps://raw.githubusercontent.com/nf-core/configs/masterIf you're running offline, Nextflow will not be able to fetch the institutional config files from the internet. If you don't need them, then this is not a problem. If you do need them, you should download the files from the repo and tell Nextflow where to find them with this parameter.
Institutional config name.
stringInstitutional config description.
stringInstitutional config contact information.
stringDirectory to keep pipeline Nextflow logs and reports.
string${params.outdir}/pipeline_infoSet the top limit for requested resources for any single job.
Maximum number of CPUs that can be requested for any single job.
integer16Use to set an upper-limit for the CPU requirement for each process. Should be an integer e.g. --max_cpus 1
Maximum amount of memory that can be requested for any single job.
string128.GB^\d+(\.\d+)?\.?\s*(K|M|G|T)?B$Use to set an upper-limit for the memory requirement for each process. Should be a string in the format integer-unit e.g. --max_memory '8.GB'
Maximum amount of time that can be requested for any single job.
string240.h^(\d+\.?\s*(s|m|h|d|day)\s*)+$Use to set an upper-limit for the time requirement for each process. Should be a string in the format integer-unit e.g. --max_time '2.h'
Less common options for the pipeline, typically set in a config file.
Display help text.
booleanDisplay version and exit.
booleanMethod used to save pipeline results to output directory.
stringThe Nextflow publishDir option specifies which intermediate files should be saved to the output directory. This option tells the pipeline what method should be used to move these files. See Nextflow docs for details.
Email address for completion summary, only when pipeline fails.
string^([a-zA-Z0-9_\-\.]+)@([a-zA-Z0-9_\-\.]+)\.([a-zA-Z]{2,5})$An email address to send a summary email to when the pipeline is completed - ONLY sent if the pipeline does not exit successfully.
Send plain-text email instead of HTML.
booleanMultiQC report title. Printed as page header, used for filename if not otherwise specified.
stringFile size limit when attaching MultiQC reports to summary emails.
string25.MB^\d+(\.\d+)?\.?\s*(K|M|G|T)?B$Do not use coloured log outputs.
booleanIncoming hook URL for messaging service
stringIncoming hook URL for messaging service. Currently, MS Teams and Slack are supported.
Custom config file to supply to MultiQC.
stringCustom logo file to supply to MultiQC. File name must also be set in the MultiQC config file
stringCustom MultiQC yaml file containing HTML including a methods description.
stringBoolean whether to validate parameters against the schema at runtime
booleantrueShow all params when using --help
booleanBy default, parameters set as hidden in the schema are not shown on the command line when a user runs with --help. Specifying this option will tell the pipeline to show all parameters.
Validation of parameters fails when an unrecognised parameter is found.
booleanBy default, when an unrecognised parameter is found, it returns a warinig.
Validation of parameters in lenient more.
booleanAllows string values that are parseable as numbers or booleans. For further information see JSONSchema docs.