diff --git a/README.md b/README.md index 3f45cba..ba4022f 100644 --- a/README.md +++ b/README.md @@ -77,8 +77,6 @@ On release, automated continuous integration tests run the pipeline on a full-si nextflow run nf-core/taxprofiler --input samplesheet.csv --databases database.csv --outdir --run_ --run_ -profile ``` -Note pipeline supports both CSV and PEP input sample sheets. Find out more [here](http://pep.databio.org/en/2.1.0/specification/). - ## Documentation The nf-core/taxprofiler pipeline comes with documentation about the pipeline [usage](https://nf-co.re/taxprofiler/usage), [parameters](https://nf-co.re/taxprofiler/parameters) and [output](https://nf-co.re/taxprofiler/output). diff --git a/assets/samplesheet_schema.yaml b/assets/samplesheet_schema.yaml deleted file mode 100644 index 88ff451..0000000 --- a/assets/samplesheet_schema.yaml +++ /dev/null @@ -1,55 +0,0 @@ -description: A schema for validation of samplesheet.csv for taxprofiler pipeline. -imports: - - https://schema.databio.org/pep/2.1.0.yaml -properties: - samples: - type: array - items: - type: object - properties: - sample: - type: string - description: "Sample identifier." - pattern: "^\\S*$" - run_accession: - type: string - description: "Run accession number." - instrument_platform: - type: string - description: "Name of the platform that sequenced the samples." - enum: - [ - "ABI_SOLID", - "BGISEQ", - "CAPILLARY", - "COMPLETE_GENOMICS", - "DNBSEQ", - "HELICOS", - "ILLUMINA", - "ION_TORRENT", - "LS454", - "OXFORD_NANOPORE", - "PACBIO_SMRT", - ] - fastq1: - type: ["string", "null"] - description: "Optional FASTQ file for read 1 of paired-end sequenced libraries." - pattern: "^[\\S]+.(fq\\.gz|fastq\\.gz)$" - fastq2: - type: ["string", "null"] - description: "Optional FASTQ file for read 2 of paired-end sequenced libraries." - pattern: "^[\\S]+.(fq\\.gz|fastq\\.gz)$" - fasta: - type: ["string", "null"] - description: "Optional FASTA file." - pattern: "^[\\S]+.(fa\\.gz|fasta\\.gz)$" - required: - - sample - - run_accession - - instrument_platform - files: - - fastq1 - - fastq2 - - fasta -required: - - samples diff --git a/bin/check_samplesheet.py b/bin/check_samplesheet.py new file mode 100755 index 0000000..ca54ed9 --- /dev/null +++ b/bin/check_samplesheet.py @@ -0,0 +1,236 @@ +#!/usr/bin/env python + +from distutils import extension +import os +import sys +import errno +import argparse + + +def parse_args(args=None): + Description = "Reformat nf-core/taxprofiler samplesheet file and check its contents." + + Epilog = "Example usage: python check_samplesheet.py " + + parser = argparse.ArgumentParser(description=Description, epilog=Epilog) + parser.add_argument("FILE_IN", help="Input samplesheet file.") + parser.add_argument("FILE_OUT", help="Output file.") + return parser.parse_args(args) + + +def make_dir(path): + if len(path) > 0: + try: + os.makedirs(path) + except OSError as exception: + if exception.errno != errno.EEXIST: + raise exception + + +def print_error(error, context="Line", context_str=""): + error_str = "ERROR: Please check samplesheet -> {}".format(error) + if context != "" and context_str != "": + error_str = "ERROR: Please check samplesheet -> {}\n{}: '{}'".format( + error, context.strip(), context_str.strip() + ) + print(error_str) + sys.exit(1) + + +def check_samplesheet(file_in, file_out): + """ + This function checks that the samplesheet follows the following structure: + + sample,run_accession,instrument_platform,fastq_1,fastq_2,fasta + 2611,ERR5766174,ILLUMINA,,,ERX5474930_ERR5766174_1.fa.gz + 2612,ERR5766176,ILLUMINA,ERX5474932_ERR5766176_1.fastq.gz,ERX5474932_ERR5766176_2.fastq.gz, + 2612,ERR5766174,ILLUMINA,ERX5474936_ERR5766180_1.fastq.gz,, + 2613,ERR5766181,ILLUMINA,ERX5474937_ERR5766181_1.fastq.gz,ERX5474937_ERR5766181_2.fastq.gz, + """ + + FQ_EXTENSIONS = (".fq.gz", ".fastq.gz") + FA_EXTENSIONS = ( + ".fa", + ".fa.gz", + ".fasta", + ".fasta.gz", + ".fna", + ".fna.gz", + ".fas", + ".fas.gz", + ) + INSTRUMENT_PLATFORMS = [ + "ABI_SOLID", + "BGISEQ", + "CAPILLARY", + "COMPLETE_GENOMICS", + "DNBSEQ", + "HELICOS", + "ILLUMINA", + "ION_TORRENT", + "LS454", + "OXFORD_NANOPORE", + "PACBIO_SMRT", + ] + + sample_mapping_dict = {} + with open(file_in, "r") as fin: + + ## Check header + MIN_COLS = 4 + HEADER = [ + "sample", + "run_accession", + "instrument_platform", + "fastq_1", + "fastq_2", + "fasta", + ] + header = [x.strip('"') for x in fin.readline().strip().split(",")] + + ## Check for missing mandatory columns + missing_columns = list(set(HEADER) - set(header)) + if len(missing_columns) > 0: + print( + "ERROR: Missing required column header -> {}. Note some columns can otherwise be empty. See pipeline documentation (https://nf-co.re/taxprofiler/usage).".format( + ",".join(missing_columns) + ) + ) + sys.exit(1) + + ## Find locations of mandatory columns + header_locs = {} + for i in HEADER: + header_locs[i] = header.index(i) + + ## Check sample entries + for line in fin: + + ## Pull out only relevant columns for downstream checking + line_parsed = [x.strip().strip('"') for x in line.strip().split(",")] + lspl = [line_parsed[i] for i in header_locs.values()] + + # Check valid number of columns per row + if len(lspl) < len(HEADER): + print_error( + "Invalid number of columns (minimum = {})!".format(len(HEADER)), + "Line", + line, + ) + num_cols = len([x for x in lspl if x]) + if num_cols < MIN_COLS: + print_error( + "Invalid number of populated columns (minimum = {})!".format(MIN_COLS), + "Line", + line, + ) + + ## Check sample name entries + + ( + sample, + run_accession, + instrument_platform, + fastq_1, + fastq_2, + fasta, + ) = lspl[: len(HEADER)] + sample = sample.replace(" ", "_") + if not sample: + print_error("Sample entry has not been specified!", "Line", line) + + ## Check FastQ file extension + for fastq in [fastq_1, fastq_2]: + if fastq: + if fastq.find(" ") != -1: + print_error("FastQ file contains spaces!", "Line", line) + if not fastq.endswith(FQ_EXTENSIONS): + print_error( + f"FastQ file does not have extension {' or '.join(list(FQ_EXTENSIONS))} !", + "Line", + line, + ) + if fasta: + if fasta.find(" ") != -1: + print_error("FastA file contains spaces!", "Line", line) + if not fasta.endswith(FA_EXTENSIONS): + print_error( + f"FastA file does not have extension {' or '.join(list(FA_EXTENSIONS))}!", + "Line", + line, + ) + sample_info = [] + + # Check run_accession + if not run_accession: + print_error("Run accession has not been specified!", "Line", line) + else: + sample_info.append(run_accession) + + # Check instrument_platform + if not instrument_platform: + print_error("Instrument platform has not been specified!", "Line", line) + else: + if instrument_platform not in INSTRUMENT_PLATFORMS: + print_error( + f"Instrument platform {instrument_platform} is not supported!", + f"List of supported platforms {', '.join(INSTRUMENT_PLATFORMS)}", + "Line", + line, + ) + sample_info.append(instrument_platform) + + ## Auto-detect paired-end/single-end + if sample and fastq_1 and fastq_2: ## Paired-end short reads + sample_info.extend(["0", fastq_1, fastq_2, fasta]) + elif sample and fastq_1 and not fastq_2: ## Single-end short/long fastq reads + sample_info.extend(["1", fastq_1, fastq_2, fasta]) + elif sample and fasta and not fastq_1 and not fastq_2: ## Single-end long reads + sample_info.extend(["1", fastq_1, fastq_2, fasta]) + elif fasta and (fastq_1 or fastq_2): + print_error( + "FastQ and FastA files cannot be specified together in the same library!", + "Line", + line, + ) + else: + print_error("Invalid combination of columns provided!", "Line", line) + + ## Create sample mapping dictionary = { sample: [ run_accession, instrument_platform, single_end, fastq_1, fastq_2 , fasta ] } + if sample not in sample_mapping_dict: + sample_mapping_dict[sample] = [sample_info] + else: + if sample_info in sample_mapping_dict[sample]: + print_error("Samplesheet contains duplicate rows!", "Line", line) + else: + sample_mapping_dict[sample].append(sample_info) + + ## Write validated samplesheet with appropriate columns + HEADER_OUT = [ + "sample", + "run_accession", + "instrument_platform", + "single_end", + "fastq_1", + "fastq_2", + "fasta", + ] + if len(sample_mapping_dict) > 0: + out_dir = os.path.dirname(file_out) + make_dir(out_dir) + with open(file_out, "w") as fout: + fout.write(",".join(HEADER_OUT) + "\n") + for sample in sorted(sample_mapping_dict.keys()): + for idx, val in enumerate(sample_mapping_dict[sample]): + fout.write(f"{sample},{','.join(val)}\n") + else: + print_error("No entries to process!", "Samplesheet: {}".format(file_in)) + + +def main(args=None): + args = parse_args(args) + check_samplesheet(args.FILE_IN, args.FILE_OUT) + + +if __name__ == "__main__": + sys.exit(main()) diff --git a/conf/modules.config b/conf/modules.config index dd85c0c..d84102c 100644 --- a/conf/modules.config +++ b/conf/modules.config @@ -495,12 +495,4 @@ process { saveAs: { filename -> filename.equals('versions.yml') ? null : filename } ] } - - withName: 'EIDO_VALIDATE' { - ext.args = '--st-index sample' - } - - withName: 'EIDO_CONVERT' { - ext.args = '--st-index sample' - } } diff --git a/conf/test.config b/conf/test.config index db9f81d..275e5a0 100644 --- a/conf/test.config +++ b/conf/test.config @@ -60,10 +60,4 @@ process { withName: MEGAN_RMA2INFO_KRONA { maxForks = 1 } - withName: 'EIDO_VALIDATE' { - ext.args = '--st-index sample' - } - withName: 'EIDO_CONVERT' { - ext.args = '--st-index sample' - } } diff --git a/conf/test_krakenuniq.config b/conf/test_krakenuniq.config index 67b559e..7ba18fa 100644 --- a/conf/test_krakenuniq.config +++ b/conf/test_krakenuniq.config @@ -63,10 +63,4 @@ process { withName: MEGAN_RMA2INFO_KRONA { maxForks = 1 } - withName: 'EIDO_VALIDATE' { - ext.args = '--st-index sample' - } - withName: 'EIDO_CONVERT' { - ext.args = '--st-index sample' - } } diff --git a/conf/test_pep.config b/conf/test_pep.config deleted file mode 100644 index 6ce788d..0000000 --- a/conf/test_pep.config +++ /dev/null @@ -1,45 +0,0 @@ -params { - config_profile_name = 'Test PEP profile' - config_profile_description = 'Minimal test dataset to check pipeline function with PEP file as an input.' - - // Limit resources so that this can run on GitHub Actions - max_cpus = 2 - max_memory = '6.GB' - max_time = '6.h' - - // Input data - input = 'https://raw.githubusercontent.com/nf-core/test-datasets/modules/data/delete_me/pep/test_pep_format_files/config.yaml' - databases = 'https://raw.githubusercontent.com/nf-core/test-datasets/taxprofiler/database.csv' - perform_shortread_qc = true - perform_longread_qc = true - perform_shortread_complexityfilter = true - perform_shortread_hostremoval = true - perform_longread_hostremoval = true - perform_runmerging = true - hostremoval_reference = 'https://raw.githubusercontent.com/nf-core/test-datasets/modules/data/genomics/homo_sapiens/genome/genome.fasta' - run_kaiju = true - run_kraken2 = true - run_bracken = true - run_malt = true - run_metaphlan3 = true - run_centrifuge = true - run_diamond = true - run_motus = false - run_krona = true - krona_taxonomy_directory = 'https://raw.githubusercontent.com/nf-core/test-datasets/modules/data/genomics/sarscov2/metagenome/krona_taxonomy.tab' - malt_save_reads = true - kraken2_save_reads = true - centrifuge_save_reads = true - diamond_save_reads = true -} - - -process { - withName: MALT_RUN { - maxForks = 1 - ext.args = { "-m ${params.malt_mode} -J-Xmx12G" } - } - withName: MEGAN_RMA2INFO { - maxForks = 1 - } -} diff --git a/docs/usage.md b/docs/usage.md index f748764..685c3e3 100644 --- a/docs/usage.md +++ b/docs/usage.md @@ -22,10 +22,6 @@ This samplesheet is then specified on the command line as follows: --input '[path to samplesheet file]' --databases '[path to database sheet file]' ``` -Note pipeline supports both CSV and PEP input sample sheets. Find out more [here](http://pep.databio.org/en/2.1.0/specification/). -When using PEP as an input, the `samplesheet.csv` must be placed in the same folder -as `config.yaml` file. A path to `samplesheet.csv` within the config must be absolute. - ### Multiple runs of the same sample The `sample` identifiers have to be the same when you have re-sequenced the same sample more than once e.g. to increase sequencing depth. The pipeline will concatenate different runs FASTQ files of the same sample before performing profiling, when `--perform_runmerging` is supplied. Below is an example for the same sample sequenced across 3 lanes: @@ -312,9 +308,6 @@ If `-profile` is not specified, the pipeline will run locally and expect all sof - `test` - A profile with a complete configuration for automated testing - Includes links to test data so needs no other parameters -- `test_pep` - - A profile with a complete configuration for running a pipeline with PEP as input - - Includes links to test data so needs no other parameters - `docker` - A generic configuration profile to be used with [Docker](https://docker.com/) - `singularity` diff --git a/lib/WorkflowMain.groovy b/lib/WorkflowMain.groovy index 93d2af3..f0107fb 100755 --- a/lib/WorkflowMain.groovy +++ b/lib/WorkflowMain.groovy @@ -81,7 +81,7 @@ class WorkflowMain { // Check input has been provided if (!params.input) { - log.error "Please provide an input samplesheet or PEP to the pipeline e.g. '--input samplesheet.csv'" + log.error "Please provide an input samplesheet to the pipeline e.g. '--input samplesheet.csv'" System.exit(1) } } diff --git a/modules.json b/modules.json index 377e902..286ab88 100644 --- a/modules.json +++ b/modules.json @@ -55,16 +55,6 @@ "git_sha": "5e34754d42cd2d5d248ca8673c0a53cdf5624905", "installed_by": ["modules"] }, - "eido/convert": { - "branch": "master", - "git_sha": "5e34754d42cd2d5d248ca8673c0a53cdf5624905", - "installed_by": ["modules"] - }, - "eido/validate": { - "branch": "master", - "git_sha": "5e34754d42cd2d5d248ca8673c0a53cdf5624905", - "installed_by": ["modules"] - }, "falco": { "branch": "master", "git_sha": "fc959214036403ad83efe7a41d43d0606c445cda", diff --git a/modules/local/samplesheet_check.nf b/modules/local/samplesheet_check.nf new file mode 100644 index 0000000..dea4362 --- /dev/null +++ b/modules/local/samplesheet_check.nf @@ -0,0 +1,27 @@ +process SAMPLESHEET_CHECK { + tag "$samplesheet" + + conda (params.enable_conda ? "conda-forge::python=3.8.3" : null) + container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ? + 'https://depot.galaxyproject.org/singularity/python:3.8.3' : + 'quay.io/biocontainers/python:3.8.3' }" + + input: + path samplesheet + + output: + path '*.csv' , emit: csv + path "versions.yml", emit: versions + + script: // This script is bundled with the pipeline, in nf-core/taxprofiler/bin/ + """ + check_samplesheet.py \\ + $samplesheet \\ + samplesheet.valid.csv + + cat <<-END_VERSIONS > versions.yml + "${task.process}": + python: \$(python --version | sed 's/Python //g') + END_VERSIONS + """ +} diff --git a/modules/nf-core/eido/convert/main.nf b/modules/nf-core/eido/convert/main.nf deleted file mode 100644 index 7ec4b8c..0000000 --- a/modules/nf-core/eido/convert/main.nf +++ /dev/null @@ -1,38 +0,0 @@ -process EIDO_CONVERT { - tag "$samplesheet" - label 'process_single' - - conda (params.enable_conda ? "conda-forge::eido=0.1.9" : null) - container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ? - 'https://containers.biocontainers.pro/s3/SingImgsRepo/eido/0.1.9_cv1/eido_0.1.9_cv1.sif' : - 'biocontainers/eido:0.1.9_cv1' }" - - input: - path samplesheet - val format - path pep_input_base_dir - - output: - path "versions.yml" , emit: versions - path "${prefix}.${format}" , emit: samplesheet_converted - - when: - task.ext.when == null || task.ext.when - - script: - def args = task.ext.args ?: '' - prefix = task.ext.prefix ?: "samplesheet_converted" - """ - eido \\ - convert \\ - -f $format \\ - $samplesheet \\ - $args \\ - -p samples=${prefix}.${format} - - cat <<-END_VERSIONS > versions.yml - "${task.process}": - eido: \$(echo \$(eido --version 2>&1) | sed 's/^.*eido //;s/ .*//' )) - END_VERSIONS - """ -} diff --git a/modules/nf-core/eido/convert/meta.yml b/modules/nf-core/eido/convert/meta.yml deleted file mode 100644 index bd12e03..0000000 --- a/modules/nf-core/eido/convert/meta.yml +++ /dev/null @@ -1,39 +0,0 @@ -name: "eido_convert" -description: Convert any PEP project or Nextflow samplesheet to any format -keywords: - - eido - - convert - - PEP - - format - - samplesheet -tools: - - "eido": - description: "Convert any PEP project or Nextflow samplesheet to any format" - homepage: "http://eido.databio.org/en/latest/" - documentation: "http://eido.databio.org/en/latest/" - doi: "10.1093/gigascience/giab077" - licence: "BSD-2-Clause" - -input: - - samplesheet: - type: file - description: Nextflow samplesheet or PEP project - pattern: "*.{yaml,yml,csv}" - - format: - type: value - description: Extension of an output file - - pep_input_base_dir: - type: file - description: Optional path to the directory where files specified in a PEP config file are stored. Any paths specified in the config will need to be relative to this base directory. - -output: - - versions: - type: file - description: File containing software versions - pattern: "versions.yml" - - samplesheet_converted: - type: file - description: PEP project or samplesheet converted to csv file - -authors: - - "@rafalstepien" diff --git a/modules/nf-core/eido/validate/main.nf b/modules/nf-core/eido/validate/main.nf deleted file mode 100644 index 798d3a0..0000000 --- a/modules/nf-core/eido/validate/main.nf +++ /dev/null @@ -1,33 +0,0 @@ -process EIDO_VALIDATE { - tag "$samplesheet" - label 'process_single' - - conda (params.enable_conda ? "conda-forge::eido=0.1.9" : null) - container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ? - 'https://containers.biocontainers.pro/s3/SingImgsRepo/eido/0.1.9_cv2/eido_0.1.9_cv2.sif' : - 'biocontainers/eido:0.1.9_cv2' }" - - input: - path samplesheet - path schema - path pep_input_base_dir - - output: - path "versions.yml" , emit: versions - path "*.log" , emit: log - - when: - task.ext.when == null || task.ext.when - - script: - def args = task.ext.args ?: '' - def prefix = task.ext.prefix ?: "validation" - """ - eido validate $args $samplesheet -s $schema -e > ${prefix}.log - - cat <<-END_VERSIONS > versions.yml - "${task.process}": - eido: \$(echo \$(eido --version 2>&1) | sed 's/^.*eido //;s/ .*//' )) - END_VERSIONS - """ -} diff --git a/modules/nf-core/eido/validate/meta.yml b/modules/nf-core/eido/validate/meta.yml deleted file mode 100644 index eb7b295..0000000 --- a/modules/nf-core/eido/validate/meta.yml +++ /dev/null @@ -1,41 +0,0 @@ -name: "eido_validate" -description: Validate samplesheet or PEP config against a schema -keywords: - - eido - - validate - - schema - - format - - pep -tools: - - "validate": - description: "Validate samplesheet or PEP config against a schema." - homepage: "http://eido.databio.org/en/latest/" - documentation: "http://eido.databio.org/en/latest/" - doi: "10.1093/gigascience/giab077" - licence: "BSD-2-Clause" - -input: - - samplesheet: - type: file - description: Samplesheet or PEP file to be validated - pattern: "*.{yaml,yml,csv}" - - schema: - type: file - description: Schema that the samplesheet will be validated against - pattern: "*.{yaml,yml}" - - pep_input_base_dir: - type: file - description: Optional path to the directory where files specified in a PEP config file are stored. Any paths specified in the config will need to be relative to this base directory. - -output: - - versions: - type: file - description: File containing software versions - pattern: "versions.yml" - - log: - type: file - description: File containing validation log. - pattern: "*.log" - -authors: - - "@rafalstepien" diff --git a/nextflow.config b/nextflow.config index 6d5a374..088bcec 100644 --- a/nextflow.config +++ b/nextflow.config @@ -252,7 +252,6 @@ profiles { test_nothing { includeConfig 'conf/test_nothing.config' } test_motus { includeConfig 'conf/test_motus.config' } test_krakenuniq { includeConfig 'conf/test_krakenuniq.config' } - test_pep { includeConfig 'conf/test_pep.config' } } diff --git a/subworkflows/local/input_check.nf b/subworkflows/local/input_check.nf index 46baff2..eb21b9d 100644 --- a/subworkflows/local/input_check.nf +++ b/subworkflows/local/input_check.nf @@ -2,41 +2,31 @@ // Check input samplesheet and get read channels // -include { EIDO_VALIDATE } from '../../modules/nf-core/eido/validate/main' -include { EIDO_CONVERT } from '../../modules/nf-core/eido/convert/main' +include { SAMPLESHEET_CHECK } from '../../modules/local/samplesheet_check' workflow INPUT_CHECK { take: - samplesheet_or_pep_config // file: /path/to/samplesheet.csv or /path/to/pep/config.yaml - pep_input_base_dir + samplesheet // file: /path/to/samplesheet.csv main: - ch_versions = Channel.empty() - - EIDO_VALIDATE ( samplesheet_or_pep_config, file("$projectDir/assets/samplesheet_schema.yaml"), pep_input_base_dir ) - ch_versions = ch_versions.mix(EIDO_VALIDATE.out.versions) - - EIDO_CONVERT ( samplesheet_or_pep_config, "csv", pep_input_base_dir ) - ch_versions = ch_versions.mix(EIDO_CONVERT.out.versions) - - ch_parsed_samplesheet = EIDO_CONVERT.out.samplesheet_converted + parsed_samplesheet = SAMPLESHEET_CHECK ( samplesheet ) + .csv .splitCsv ( header:true, sep:',' ) - .map { check_missing_and_singleend_autodetect(it) } .branch { fasta: it['fasta'] != '' nanopore: it['instrument_platform'] == 'OXFORD_NANOPORE' fastq: true } - ch_parsed_samplesheet.fastq + parsed_samplesheet.fastq .map { create_fastq_channel(it) } .set { fastq } - ch_parsed_samplesheet.nanopore + parsed_samplesheet.nanopore .map { create_fastq_channel(it) } .set { nanopore } - ch_parsed_samplesheet.fasta + parsed_samplesheet.fasta .map { create_fasta_channel(it) } .set { fasta } @@ -44,20 +34,7 @@ workflow INPUT_CHECK { fastq = fastq ?: [] // channel: [ val(meta), [ reads ] ] nanopore = nanopore ?: [] // channel: [ val(meta), [ reads ] ] fasta = fasta ?: [] // channel: [ val(meta), fasta ] - versions = ch_versions // channel: [ versions.yml ] -} - -// Function to validate input sheet and auto-detect R1/R2 -def check_missing_and_singleend_autodetect(LinkedHashMap row) { - - // Checks not supported by EIDO(?) - if ( ( row['fastq_1'] != "" || row['fastq_2'] != "" ) && row['fasta'] != "" ) { exit 1, "[nf-core/taxprofiler] ERROR: FastQ and FastA files cannot be specified together in the same library. Check input samplesheet! Check sample: ${row['sample']}" } - if ( row['fastq_1'] == "" && row['fastq_2'] != "" ) { exit 1, "[nf-core/taxprofiler] ERROR: Input samplesheet has a missing fastq_1 when fastq_2 is specified. Check sample: ${row['sample']}" } - - single_end = row['fastq_2'] == "" ? true : false - row['single_end'] = single_end - - return row + versions = SAMPLESHEET_CHECK.out.versions // channel: [ versions.yml ] } // Function to get list of [ meta, [ fastq_1, fastq_2 ] ] @@ -87,12 +64,11 @@ def create_fastq_channel(LinkedHashMap row) { if (!file(row.fastq_2).exists()) { exit 1, "ERROR: Please check input samplesheet -> Read 2 FastQ file does not exist!\n${row.fastq_2}" } - fastq_meta = [ meta, [ file(row.fastq_1), file(row.fastq_2) ] ] + fastq_meta = [ meta, [ file(row.fastq_1), file(row.fastq_2) ] ] } } return fastq_meta - }// Function to get list of [ meta, fasta ] def create_fasta_channel(LinkedHashMap row) { def meta = [:] diff --git a/workflows/taxprofiler.nf b/workflows/taxprofiler.nf index c9f002c..73aa0ef 100644 --- a/workflows/taxprofiler.nf +++ b/workflows/taxprofiler.nf @@ -20,9 +20,8 @@ for (param in checkPathParamList) { if (param) { file(param, checkIfExists: true // Check mandatory parameters if ( params.input ) { ch_input = file(params.input, checkIfExists: true) - pep_input_base_dir = file(params.input).extension.matches("yaml|yml") ? file(file(params.input).getParent(), checkIfExists: true) : [] } else { - exit 1, "Input samplesheet, or PEP config and base directory not specified" + exit 1, "Input samplesheet not specified" } if (params.databases) { ch_databases = file(params.databases) } else { exit 1, 'Input database sheet not specified!' } @@ -115,7 +114,7 @@ workflow TAXPROFILER { SUBWORKFLOW: Read in samplesheet, validate and stage input files */ INPUT_CHECK ( - ch_input, pep_input_base_dir + ch_input ) ch_versions = ch_versions.mix(INPUT_CHECK.out.versions)