nf-core/scnanoseq
Single-cell/nuclei pipeline for data derived from Oxford Nanopore and 10X Genomics
1.1.0). The latest
stable release is
1.2.1
.
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+\.csv$The output directory where the results will be saved. You have to use absolute paths to storage on Cloud infrastructure.
stringEmail address for completion summary.
string^([a-zA-Z0-9_\-\.]+)@([a-zA-Z0-9_\-\.]+)\.([a-zA-Z]{2,5})$MultiQC report title. Printed as page header, used for filename if not otherwise specified.
stringReference genome related files and options required for the workflow.
Path to genome FASTA file.
string^\S+\.fn?a(sta)?(\.gz)?$Path to transcriptome FASTA file.
string^\S+\.fn?a(sta)?(\.gz)?$Path to GTF file.
string^\S+\.gtf(\.gz)?$Name of iGenomes reference.
stringDo not load the iGenomes reference config.
booleantrueThe base path to the igenomes reference files
strings3://ngi-igenomes/igenomes/This is the delimiter the FASTA uses in the sequence identifier to separate the string.
stringOptions related to processing fastqs
The amount of lines to split the FASTQ into.
integerOptions to choose trimming criteria and software.
Choose minimum read length.
integer1Choose minimum average read quality score.
integer10Skip quality trimming step.
booleanOptions related to the barcode and umis.
User-provided file containing a list of cellular barcodes. Using this parameter will override the default whitelists provided by the pipeline and use the user-provided one instead.
stringSpecify the format for the barcode+umi. This parameter also defines a default barcode whitelist for the pipeline to use for barcode calling, this can be overidden with the ‘whitelist’ parameter.
stringSpecify which tool to be used for deduplication (Options: picard, umitools)
stringOptions related to minimap2.
Library strandness option.
stringMinimizer k-mer length.
integer14Save the secondary alignments when aligning to the genome
booleanSave the secondary alignments when aligning to the transcriptome
booleantrueOptions related to post-mapping analysis
Indicate whether to include introns in the count matrices
booleantrueProvide a comma-delimited options of quantifiers for the pipeline to use. Available tools: isoquant, oarfish
stringOptions to skip various steps within the workflow.
Skip all QC.
booleanSkip FastQC.
booleanSkip Nanoplot.
booleanSkip ToulligQC.
booleanSkip NanoComp from FASTQ file(s).
booleanSkip NanoComp from BAM file(s).
booleanSkip RSeQC.
booleanSkip Seurat QC.
booleanSkip saving minimap2 index.
booleanSkip umi dedup.
booleanSkip MultiQC.
booleanParameters 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/masterInstitutional config name.
stringInstitutional config description.
stringInstitutional config contact information.
stringInstitutional config URL link.
stringLess common options for the pipeline, typically set in a config file.
Display version and exit.
booleanMethod used to save pipeline results to output directory.
stringEmail address for completion summary, only when pipeline fails.
string^([a-zA-Z0-9_\-\.]+)@([a-zA-Z0-9_\-\.]+)\.([a-zA-Z]{2,5})$Send plain-text email instead of HTML.
booleanFile 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
stringCustom 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
booleantrueBase URL or local path to location of pipeline test dataset files
stringhttps://raw.githubusercontent.com/nf-core/test-datasets/