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nf_cutntag
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nf_cutntag
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#!/usr/bin/env nextflow
nextflow.enable.dsl=2
/* ========================================================================================
OUTPUT DIRECTORY
======================================================================================== */
params.outdir = false
if(params.outdir){
outdir = params.outdir
} else {
outdir = '.'
}
/* ========================================================================================
PARAMETERS
======================================================================================== */
params.fastqc_args = ''
params.fastq_screen_args = ''
params.trim_galore_args = ''
params.bowtie2_args = ''
params.samtools_sort_args = ''
params.samtools_index_args = ''
params.mark_duplicates_args = ''
params.bedtools_genomecov_args = ''
params.multiqc_args = ''
params.genome = ''
params.verbose = false
params.single_end = false // default mode is auto-detect. NOTE: params are handed over automatically
params.help = false
params.list_genomes = false
/* ========================================================================================
MESSAGES
======================================================================================== */
// Show help message and exit
if (params.help){
helpMessage()
exit 0
}
if (params.list_genomes){
println ("[WORKLFOW] List genomes selected")
}
if (params.verbose){
println ("[WORKFLOW] FASTQC ARGS: " + params.fastqc_args)
println ("[WORKFLOW] FASTQ SCREEN ARGS ARE: " + params.fastq_screen_args)
println ("[WORKFLOW] TRIM GALORE ARGS: " + params.trim_galore_args)
println ("[WORKFLOW] BOWTIE2 ARGS: " + params.bowtie2_args)
println ("[WORKFLOW] SAMTOOLS SORT ARGS: " + params.samtools_sort_args)
println ("[WORKFLOW] SAMTOOLS INDEX ARGS: " + params.samtools_index_args)
println ("[WORKFLOW] MARK_DUPLICATES ARGS: " + params.mark_duplicates_args)
println ("[WORKFLOW] BEDTOOLS GENOMECOV ARGS: " + params.bedtools_genomecov_args)
println ("[WORKFLOW] MULTIQC ARGS: " + params.multiqc_args)
}
/* ========================================================================================
GENOMES
======================================================================================== */
include { getGenome; listGenomes } from './nf_modules/genomes.mod.nf'
if (params.list_genomes){
listGenomes() // this lists all available genomes, and exits
}
genome = getGenome(params.genome)
/* ========================================================================================
FILES CHANNEL
======================================================================================== */
include { makeFilesChannel; getFileBaseNames } from './nf_modules/files.mod.nf'
file_ch = makeFilesChannel(args)
/* ========================================================================================
WORKFLOW
======================================================================================== */
// ---------------------------------------- //
// Condition to output the original sorted.bam file only if that file will be subsequently deduplicated
// With deduplication, outputs: *.sorted.bam and *.sorted.dedup.bam
// Without deduplication, outputs: *.sorted.dupflag.bam
if ((params.mark_duplicates_args =~ /.*REMOVE_DUPLICATES=true.*/) || (params.mark_duplicates_args =~ /.*REMOVE_SEQUENCING_DUPLICATES=true.*/)){
params.bam_output = true
} else {
params.bam_output = false
}
// ---------------------------------------- //
include { FASTQC } from './nf_modules/fastqc.mod.nf'
include { FASTQC as FASTQC2 } from './nf_modules/fastqc.mod.nf'
include { FASTQ_SCREEN } from './nf_modules/fastq_screen.mod.nf'
include { TRIM_GALORE } from './nf_modules/trim_galore.mod.nf'
include { BOWTIE2 } from './nf_modules/bowtie2.mod.nf' params(bam_output: false, genome: genome, cutntag: true)
include { SAMTOOLS_SORT } from './nf_modules/samtools.mod.nf' params(bam_output: params.bam_output)
include { SAMTOOLS_INDEX } from './nf_modules/samtools.mod.nf' params(bam_output: params.bam_output)
include { MARK_DUPLICATES } from './nf_modules/picard.mod.nf' params(bam_output: params.bam_output)
include { BEDTOOLS_GENOMECOV } from './nf_modules/bedtools.mod.nf' params(genome: genome, cutntag: true)
include { MULTIQC } from './nf_modules/multiqc.mod.nf'
workflow {
main:
FASTQC (file_ch, outdir, params.fastqc_args, params.verbose)
FASTQ_SCREEN (file_ch, outdir, params.fastq_screen_args, params.verbose)
TRIM_GALORE (file_ch, outdir, params.trim_galore_args, params.verbose)
FASTQC2 (TRIM_GALORE.out.reads, outdir, params.fastqc_args, params.verbose)
BOWTIE2 (TRIM_GALORE.out.reads, outdir, params.bowtie2_args, params.verbose)
SAMTOOLS_SORT (BOWTIE2.out.bam, outdir, params.samtools_sort_args, params.verbose)
MARK_DUPLICATES (SAMTOOLS_SORT.out.bam, outdir, params.mark_duplicates_args, params.verbose)
SAMTOOLS_INDEX (MARK_DUPLICATES.out.bam, outdir, params.samtools_index_args, params.verbose)
BEDTOOLS_GENOMECOV (MARK_DUPLICATES.out.bam, outdir, params.bedtools_genomecov_args, params.verbose)
// merging channels for MultiQC
multiqc_ch = FASTQC.out.report.mix(
TRIM_GALORE.out.report,
FASTQ_SCREEN.out.report.ifEmpty([]),
FASTQC2.out.report.ifEmpty([]),
BOWTIE2.out.stats.ifEmpty([]),
MARK_DUPLICATES.out.metrics.ifEmpty([]),
).collect()
MULTIQC (multiqc_ch, outdir, params.multiqc_args, params.verbose)
}
workflow.onComplete {
def msg = """\
Pipeline execution summary
---------------------------
Jobname : ${workflow.runName}
Completed at: ${workflow.complete}
Duration : ${workflow.duration}
Success : ${workflow.success}
workDir : ${workflow.workDir}
exit status : ${workflow.exitStatus}
"""
.stripIndent()
sendMail(to: "${workflow.userName}@ethz.ch", subject: 'Minimal pipeline execution report', body: msg)
}
/* ========================================================================================
HELP MESSAGE
======================================================================================== */
def helpMessage() {
log.info"""
>>
SYNOPSIS:
In a nutshell, this workflow runs an entire processing pipeline on FastQ files, including QC, contamination QC,
quality-/adapter trimming, alignments to a genome using Bowtie 2, sorting, marking duplicates, generating a genome coverage bedgraph,
and finally generating an aggregate QC report. The workflow is suitable for CUT&Tag. Here is a graphical representation of the workflow:
--- FastQC
--- FastQ Screen
--- Trim Galore
|
--- FastQC
--- Bowtie 2
|
--- Samtools sort
--- Mark duplicates
--- Samtools index
|
--- Bedtools genomecov
--- MultiQC*
* This step runs only once ALL other jobs have completed.
By default, the involved tools are run in the following way:
------------------------------------------------------------
FastQC: defaults (-q)
FastQ Screen: defaults (Bowtie 2; local mode)
Trim Galore: defaults (adapter auto-detection)
Bowtie 2: end-to-end mode; '--no-unal'; for paired-end files: '--no-mixed --no-discordant' (concordant PE alignmnents only); '--local --very-sensitive --phred33 -I 10 -X 700'
Samtools sort defaults
Samtools index defaults
Mark duplicates defaults (ASSUME_SORTED=true)
Bedtools genomecov defaults (-bga -ibam)
To add additional parameters to any of the programs, consider supplying tool-specific arguments (see --toolname_args="..." below).
==============================================================================================================
USAGE:
nf_cutntag [options] --genome <genomeID> <input files>
Mandatory arguments:
====================
<input files> List of input files, e.g. '*fastq.gz' or '*fq.gz'. Files are automatically processed as
single-end (SE) or paired end (PE) files (if file pairs share the same base-name, and differ only
by a read number, e.g. 'base_name_R1.fastq.gz' and 'base_name_R2.fastq.gz' (or R3, R4). For
PE files, only Read 1 is run through FastQ Screen (as typically R1 and R2 produce nearly identical
contamination profiles). To run PE files in single-end mode, please see '--single_end' below.
--genome [str] Genome build ID to be used for the alignment, e.g. GRCh38 (latest human genome) or GRCm38
(latest mouse genome build). To list all available genomes, see '--list_genomes' below.
Tool-specific options:
======================
For all following options, please note that the format: ="your options" needs to be strictly adhered to in order to work correctly.
--fastqc_args="[str]" This option can take any number of options that are compatible with FastQC to modify its default
behaviour. For more detailed information on available options please refer to the FastQC documentation,
or run 'fastqc --help' on the command line. As an example, to run FastQC without grouping of bases when
reads are >50bp and use a specific file with non-default adapter sequences, use:
' --fastqc_args="--nogroup --adapters ./non_default_adapter_file.txt" '. [Default: None]
--fastq_screen_args="[str]" This option can take any number of options that are compatible with FastQ Screen to modify its
default behaviour. For more detailed information on available options please refer to the FastQ Screen
documentation, or run 'fastq_screen --help' on the command line. For instance, to process a bisulfite
converted library with fairly relaxed parameters, you could use:
' --fastq_screen_args="--bisulfite --score_min L,0,-0.6" '. [Default: None]
--trim_galore_args="[str]" This option can take any number of options that are compatible with Trim Galore to modify its
default trimming behaviour. For more detailed information on available options please refer
to the Trim Galore User Guide, or run 'trim_galore --help' on the command line. As an example, to trim
off the first 10bp from the 5' of R1 and 5bp of R2, use:
' --trim_galore_args="--clip_r1 10 --clip_r2 5" '. [Default: None]
--bowtie2_args="[str]" This option can take any number of options that are compatible with Bowtie 2 to modify its
default mapping behaviour. For more detailed information on available options please refer
to the Bowtie 2 User Guide, or run 'bowtie2 --help' on the command line. As an example, to
run somewhat more stringent alignments for only 1 million sequences, use:
' --bowtie2_args="-u 1000000 --score_min L,0,-0.4" '. [Default: None]
--samtools_sort_args="[str]" This option can take any number of options that are compatible with 'samtools sort' to modify its default
behaviour. For more detailed information on available options please refer to the Samtools documentation,
or run 'samtools sort' on the command line. Please note that the format ="your options" needs to be
strictly adhered to in order to work correctly. [Default: None]
--samtools_index_args="[str]" This option can take any number of options that are compatible with 'samtools index' to modify its
default behaviour. For more detailed information on available options please refer
to the Samtools documentation, or run 'samtools index' on the command line. Please note that the format
="your options" needs to be strictly adhered to in order to work correctly. [Default: None]
--mark_duplicates_args="[str]" This option can take any number of options that are compatible with 'picard MarkDuplicates' to modify its default
behaviour. For more detailed information on available options please refer to the picard documentation,
or run 'picard MarkDuplicates' on the command line. Please note that the format ="your options" needs to be
strictly adhered to in order to work correctly. [Default: None]
--bedtools_genomecov_args="[str]" This option can take any number of options that are compatible with 'bedtools genomecov' to modify its default
behaviour. For more detailed information on available options please refer to the bedtools documentation,
or run 'bedtools genomecov' on the command line. Please note that the format ="your options" needs to be
strictly adhered to in order to work correctly. [Default: None]
Other options:
==============
--outdir [str] Path to the output directory. [Default: current working directory]
--list_genomes List all genome builds that are currently available to choose from. To see this list
of available genomes with more detailed information about paths and indexes, run
the command as '--list_genomes --verbose'
--single_end Force files of a read pair to be treated as single-end files. [Default: auto-detect]
--verbose More verbose status messages. [Default: OFF]
--help Displays this help message and exits.
Workflow options:
=================
Please note the single '-' hyphen for the following options!
-resume If a pipeline workflow has been interrupted or stopped (e.g. by accidentally closing a laptop),
this option will attempt to resume the workflow at the point it got interrupted by using
Nextflow's caching mechanism. This may save a lot of time.
-bg Sends the entire workflow into the background, thus disconnecting it from the terminal session.
This option launches a daemon process (which will keep running on the headnode) that watches over
your workflow, and submits new jobs to the SLURM queue as required. Use this option for big pipeline
jobs, or whenever you do not want to watch the status progress yourself. Upon completion, the
pipeline will send you an email with the job details. This option is HIGHLY RECOMMENDED!
-process.executor=local Temporarily changes where the workflow is executed to the 'local' machine. See also Nextflow config
file for more details. [Default: slurm]
<<
""".stripIndent()
}