airrflow

Fasta file with adapter sequences to be trimmed.

Number of bases to clip 5' in R1 reads.

Number of bases to clip 5' in R2 reads.

Option to save trimmed reads.

Number of bases to clip 3' in R1 reads.

Number of bases to clip 3' in R2 reads.

Whether to trim adapters in fastq reads with fastp.

Trim adapters specific for Nextseq sequencing

Name of the field used to collapse duplicated sequences.

Whether to run the process to detect contamination.

Whether to apply the chimera removal filter.

Set the clustering threshold Hamming distance value. Default: 'auto'

Name of the field used to group data files to identify clones.

Name of the field used to identify external groups used to identify a clonal threshold.

Lineage tree software to use to build trees within Dowser. If you change the default, also set the lineage_tree_exec parameter.

Path to lineage tree building executable.

Perform clonal lineage tree analysis.

Name of the field used to determine if a sample is single cell sequencing or not.

Skip report of EnchantR DefineClones for all samples together.

Skip all clonal anlaysis processes

Skip report of EnchantR FindThreshold for all samples together.

Display the help message.

Display the full detailed help message.

Display hidden parameters in the help message (only works when --help or --help_full are provided).

Name of the field used to group data files to infer genotype.

Perform TIgGER novel allele and genotype inference.

Threshold for determining if two sequences come from the same clone or not.

Perform TIgGER novel allele inference.

Keep only one representative sequence per clone to perform genotype inference.

Email address for completion summary.

Path to comma-separated file containing information about the samples in the experiment.

Path to MiAIRR-BioSample mapping

Specify the processing mode for the pipeline. Available options are "fastq" and "assembled".

The output directory where the results will be saved. You have to use absolute paths to storage on Cloud infrastructure.

Indicate if C region primers are in the R1 or R2 reads.

Start position of C region primers (without counting the UMI barcode).

Path to a fasta file containing the C-region primer sequences.

Specify 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.

Start position of V region primers (without counting the UMI barcode).

Path to a fasta file containinc the V-region primer sequences.

Protocol used for the V(D)J amplicon sequencing library generation.

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).

Custom report style file in css format.

Custom logo for the report.

Custom logo for the EnchantR reports.

Custom report Rmarkdown file.

Skip multiqc report.

Skip repertoire analysis and report generation.

path to the barcode whitelist.

Specifies which read holds the barcodes

Specifies where in the read the barcodes and UMIs can be found.

Indicate if UMI indices are recorded in the R1 (default) or R2 fastq file.

Align internal C-region for a more precise isotype characterization.

Use AssemblePairs sequential instead of AssemblePairs align when assembling read pairs.

Maximum error for building the sequence consensus in the pRESTO BuildConsensus step.

Maximum gap for building the sequence consensus in the pRESTO BuildConsensus step.

Cluster sequences by similarity regardless of any annotation with pRESTO ClusterSets and annotate the cluster ID additionally to the UMI barcode.

Mask mode for C-region alignment.

Maximum allowed error when aligning the internal C-region.

Maximum allowed length when aligning the internal C-region.

Quality threshold for pRESTO FilterSeq sequence filtering.

Provide internal C-region sequences for a more precise C-region characterization. Then also set the align_cregion flag.

Align primers instead of scoring them. Used for protocols without primer fixed positions.

Use MaskPrimers align for a 5' RACE protocol.

Use when primer sequences are unknown but when their approximate positions are known.

Maximum error for building the primer consensus in the pRESTO Buildconsensus step.

Maximum allowed primer length when aligning the primers.

R1 primer extract length when using --maskprimers_extract.

Masking mode for R1 primers.

Maximum allowed error for R1 primer alignment.

R2 primer extract length when using --maskprimers_extract.

Masking mode for R2 primers.

Maximum allowed error for R2 primer alignment.

Skip filter step after alignment that ensures that locus should match the v_call chain, the sequence alignment should have at least 200 informative positions (excluding N or gaps), and maximum 10% N nucleotides in the alignment.

Path to the reference directory required by cellranger. Can either be directory or tar.gz.

BCR or TCR chains to include for embedding.

Generate sequence embeddings with amulety.

Generate a sequence amino acid translation with IgBlast.

Use GPU to generate embeddings.

Indicate if UMI indices are recorded in a separate index file.

UMI barcode length in nucleotides. Set to 0 if no UMIs present.

Indicate if UMI indices are recorded in the R1 (default) or R1 fastq file.

UMI barcode start position in the index read.

Fetch the selected germline reference bundle at runtime instead of using cached reference inputs.

Subset to productive sequences.

Whether to reassign genes if the input file is an AIRR formatted tabulated file.

Path to the germline reference fasta.

Path to the cached igblast database.

Save germline database to reuse the cache in future runs.