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.

required
type: string
pattern: ^\S+\.csv$

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

required
type: string

Email address for completion summary.

type: string
pattern: ^([a-zA-Z0-9_\-\.]+)@([a-zA-Z0-9_\-\.]+)\.([a-zA-Z]{2,5})$

MultiQC report title. Printed as page header, used for filename if not otherwise specified.

type: string

If not using the 10X Genomics platform, a custom barcode whitelist can be used with --barcode_whitelist.

type: string

Name of the tool to use for scRNA (pseudo-) alignment.

type: string

The protocol that was used to generate the single cell data, e.g. 10x Genomics v2 Chemistry.

Can be ‘auto’ (cellranger only), ‘10XV1’, ‘10XV2’, ‘10XV3’, ‘10XV4’, or any other protocol string that will get directly passed the respective aligner.

type: string
default: auto

This section can be used to disable certain tools in the pipeline

Skip MultiQC Report

type: boolean

Skip FastQC

type: boolean

Skip custom empty drops filter module

type: boolean

Reference genome related files and options required for the workflow.

Name of iGenomes reference.

type: string

Path to FASTA genome file.

type: string
pattern: ^\S+\.fn?a(sta)?(\.gz)?$

Do not load the iGenomes reference config.

hidden
type: boolean

A cDNA FASTA file

type: string

Reference GTF annotation file

type: string

Specify this parameter to save the indices created (STAR, Kallisto, Salmon) to the results.

type: boolean

Directory / URL base for iGenomes references.

hidden
type: string
default: s3://ngi-igenomes/igenomes/

This can be used to specify a precomputed Salmon index in the pipeline, in order to skip the generation of required indices by Salmon itself.

type: string

Path to transcript to gene mapping file. This allows the specification of a transcript to gene mapping file for Salmon Alevin and AlevinQC.

type: string

It is the target read length the index will be built for, using simpleaf.

type: integer
default: 91

Specify a path to the precomputed STAR index.

type: string

Ignore the SJDB GTF file.

type: string

Name of sequencing center for BAM read group tag.

type: string

Quantification type of different transcriptomic feature. Use GeneFull on pre-mRNA count for single-nucleus RNA-seq reads. Use Gene Velocyto to generate RNA velocity matrix.

type: string

Params related to Kallisto/BUS tool

Specify a path to the precomputed Kallisto index.

type: string

Specify a path to the cDNA transcripts-to-capture.

type: string

Specify a path to the intron transcripts-to-capture.

type: string

Type of workflow. Use nac for an index type that can quantify nascent and mature RNA. Use lamanno for RNA velocity based on La Manno et al. 2018 logic. (default: standard)

type: string

Activate Kallisto/BUStools filtering algorithm

type: boolean

Params related to the Cellranger pipeline

Specify a pre-calculated cellranger index. Readily prepared indexes can be obtained from the 10x Genomics website.

type: string

Should it skip the automatic renaming included in cellranger-related modules?

type: boolean

Params related to the Cellranger pipeline

Specify a motif file to create a cellranger-arc index. Can be taken, e.g., from the JASPAR database.

type: string

Specify a config file to create the cellranger-arc index.

type: string

Specify the genome reference name used in the config file to create a cellranger-arc index.

type: string

Params related to the Cellranger pipeline

Specify a pre-calculated cellranger index. Readily prepared indexes can be obtained from the 10x Genomics website.

type: string

Specify a pre-built Cell Ranger index for VDJ analysis.

type: string

Skip mkvdjref if not using VDJ data with cellranger/multi

type: boolean

Provide a probe set for fixed RNA-seq profiling (used with FFPE samples). Please refer to the 10x documentation about probesets for more details.

type: string

Provide a panel description for targeted sequencing.

type: string

Provide a Cell Multiplexing Oligo (CMO) description file when working with multiplexed samples. This is only necessary if you with to override Cell Ranger’s default CMO-set. Please refer to the 10x documentation about CMO references for more details.

type: string

Provide a reference file for feature barcoding (e.g. antibody measurements). Please refer to the Cell Ranger Feature Reference documentation for more details.

type: string

This argument takes a .txt file containing primer sequences that were used to enrich cDNA for V(D)J sequences. This is only necessary if you with to override Cell Ranger’s defaults.

type: string

This is only necessary to override Cell Ranger’s default cell calling and tag calling steps. In most cases you need to only use the cellranger_multi_barcodes parameter. Please refer to the 10x documentation for more information about this file.

type: string

Additional samplesheet to provide information about multiplexed samples. See the ‘Usage’ section for more details.

type: string

Parameters used to describe centralised config profiles. These should not be edited.

Git commit id for Institutional configs.

hidden
type: string
default: master

Base directory for Institutional configs.

hidden
type: string
default: https://raw.githubusercontent.com/nf-core/configs/master

Institutional config name.

hidden
type: string

Institutional config description.

hidden
type: string

Institutional config contact information.

hidden
type: string

Institutional config URL link.

hidden
type: string

Set the top limit for requested resources for any single job.

Maximum number of CPUs that can be requested for any single job.

hidden
type: integer
default: 16

Maximum amount of memory that can be requested for any single job.

hidden
type: string
default: 128.GB
pattern: ^\d+(\.\d+)?\.?\s*(K|M|G|T)?B$

Maximum amount of time that can be requested for any single job.

hidden
type: string
default: 240.h
pattern: ^(\d+\.?\s*(s|m|h|d|day)\s*)+$

Less common options for the pipeline, typically set in a config file.

Display help text.

hidden
type: boolean

Display version and exit.

hidden
type: boolean

Method used to save pipeline results to output directory.

hidden
type: string

Email address for completion summary, only when pipeline fails.

hidden
type: string
pattern: ^([a-zA-Z0-9_\-\.]+)@([a-zA-Z0-9_\-\.]+)\.([a-zA-Z]{2,5})$

Send plain-text email instead of HTML.

hidden
type: boolean

File size limit when attaching MultiQC reports to summary emails.

hidden
type: string
default: 25.MB
pattern: ^\d+(\.\d+)?\.?\s*(K|M|G|T)?B$

Do not use coloured log outputs.

hidden
type: boolean

Incoming hook URL for messaging service

hidden
type: string

Custom config file to supply to MultiQC.

hidden
type: string

Custom logo file to supply to MultiQC. File name must also be set in the MultiQC config file

hidden
type: string

Custom MultiQC yaml file containing HTML including a methods description.

type: string

Boolean whether to validate parameters against the schema at runtime

hidden
type: boolean
default: true

Show all params when using --help

hidden
type: boolean

Validation of parameters fails when an unrecognised parameter is found.

hidden
type: boolean

Validation of parameters in lenient more.

hidden
type: boolean

Base URL or local path to location of pipeline test dataset files

hidden
type: string
default: https://raw.githubusercontent.com/nf-core/test-datasets/