nf-core/sammyseq
Pipeline for Sequential Analysis of MacroMolecules accessibilitY sequencing (SAMMY-seq) data, to analyze chromatin state.
Parameters specific to deeptools/bigwigcompare module
A small number to avoid x/0. Only useful together with –operation log2 or –operation ratio.
number1e-14Specifies mathematical operation applied to sample fractions.
stringlog2Avoids interpretation of non-covered regions as zeros.
booleantrueWrite out all bins (of size –binSize).
booleanDefine 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$Fraction comparisons per experimentalID (e.g., “S2SvsS3” or “S2SvsS3,S2LvsS3”)
stringPath to comma-separated file containing the sample names for the desired paired comparisons.
stringThe output directory where the results will be saved. You have to use absolute paths to storage on Cloud infrastructure.
stringEmail address for completion summary.
string^([a-zA-Z0-9_\-\.]+)@([a-zA-Z0-9_\-\.]+)\.([a-zA-Z]{2,5})$MultiQC report title. Printed as page header, used for filename if not otherwise specified.
stringReference genome related files and options required for the workflow.
Name of iGenomes reference.
stringPath to FASTA genome file.
string^\S+\.fn?a(sta)?(\.gz)?$Do not load the iGenomes reference config.
booleantrueThe base path to the igenomes reference files
strings3://ngi-igenomes/igenomesSpecify aligner to be used to map reads to reference genome.
stringSpecify the tool to be used to generate comparisons
stringSpecify the program to use for read trimming
stringPath to directory or tar.gz archive for pre-built BWA index.
stringIf generated by the pipeline save the aligner index (e.g. BWA) in the results directory.
booleanPath to directory or tar.gz archive for pre-built bowtie2 index.
stringIf generated by the pipeline save the BWA index in the results directory.
booleanA BED or GTF file containing regions that should be excluded from all analyses.
stringParameters used to describe centralised config profiles. These should not be edited.
Git commit id for Institutional configs.
stringmasterBase directory for Institutional configs.
stringhttps://raw.githubusercontent.com/nf-core/configs/masterInstitutional config name.
stringInstitutional config description.
stringInstitutional config contact information.
stringInstitutional config URL link.
stringLess common options for the pipeline, typically set in a config file.
Display version and exit.
booleanMethod used to save pipeline results to output directory.
stringEmail address for completion summary, only when pipeline fails.
string^([a-zA-Z0-9_\-\.]+)@([a-zA-Z0-9_\-\.]+)\.([a-zA-Z]{2,5})$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
stringSkip MultiQC.
booleanCustom 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/Specify after which step the pipeline should stop.
stringbooleanSuffix to add to the trace report filename. Default is the date and time in the format yyyy-MM-dd_HH-mm-ss.
string“Sequencing platform identifier for BAM read group header
stringILLUMINADefines how much the reads should be extended
integerbw_resolution (expressed in base pairs) for genome coverage calculation (default 1).
integer1Method selecte to perform the normalizazion
stringEstimated genome size to performing the normalization
integerA list of space-delimited chromosome names containing those chromosomes that should be excluded for computing the normalization
stringA list of regions that will be kept in the output after filtering the alignment with samtools using -L option in addition to the flag and quality threshold filters
stringskip alignments with MAPQ smaller than ‘value’ (1 default)
integer1If set filter reads based on specific flags. Flags represent various properties of a read, such as whether it’s mapped, paired, or properly aligned (default 1540)
integer1540Region of the genome to limit the operation to - this is useful when testing parameters to reduce the computing time. The format is chr:start:end, for example –region chr10 or –region chr10:456700:891000.
stringThe number of bins that are sampled from the genome, for which the overlapping number of reads is computed. (Default: 500000)
integer500000Deeptools multiBamSummary bam bin size (Default 50000).
integerDeeptools Correlation Plot statistical calculation method
stringFragment size parameter for single-end data. When set to a positive value, it enables the —extendReads option in DeepTools, extending reads to the specified length. This parameter is only used for single-end data processing and does not affect paired-end data analysis.
integer100Optionally provide chromosome sizes file as input
stringOptionally provide FASTA index (.fai) file as input
stringPath to GTF annotation file.
stringEnable deepTools plotFingerprint analysis for quality control assessment
booleanPath to BED file containing gene intervals. This will be created from the GTF file if not specified.
stringPath to BED file containing TSS regions
string