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Hi,
I have tried to install and run nanoseq on our HPC and got the following error when trying to run the test:
Error executing process > 'NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz)' Caused by: Process `NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz)` terminated with an error exit status (127) Command executed: ## Unzip fastq file ## qcat doesnt support zipped files yet FILE=sample_nobc_dx.fastq.gz if [[ $FILE == *.gz ]] then zcat sample_nobc_dx.fastq.gz > unzipped.fastq FILE=unzipped.fastq fi qcat \ -f $FILE \ -b ./fastq \ --kit NBD103/NBD104 \ --min-score 60 \ ## Zip fastq files (cannot find pigz command) gzip fastq/* cat <<-END_VERSIONS > versions.yml "NFCORE_NANOSEQ:NANOSEQ:QCAT": qcat: $(qcat --version 2>&1 | sed 's/^.*qcat //; s/ .*$//') END_VERSIONS Command exit status: 127 Command output: (empty) Command error: .command.sh: line 11: qcat: command not found Work dir: /scratch/prj/ppn_microglia_mod/directrna/scripts/work/d4/80e29c7e90053a9789ef55a7104488 Tip: view the complete command output by changing to the process work dir and entering the command `cat .command.out`
Any help would be appreciated!
$ nextflow run nf-core/nanoseq -profile test, singularity N E X T F L O W ~ version 22.10.1 Launching `https://github.com/nf-core/nanoseq` [goofy_bernard] DSL2 - revision: 6e563e5436 [master] ------------------------------------------------------ ,--./,-. ___ __ __ __ ___ /,-._.--~' |\ | |__ __ / ` / \ |__) |__ } { | \| | \__, \__/ | \ |___ \`-._,-`-, `._,._,' nf-core/nanoseq v3.1.0-g6e563e5 ------------------------------------------------------ Core Nextflow options revision : master runName : goofy_bernard launchDir : /scratch/prj/ppn_microglia_mod/directrna/scripts workDir : /scratch/prj/ppn_microglia_mod/directrna/scripts/work projectDir : /users/k19022845/.nextflow/assets/nf-core/nanoseq userName : k19022845 profile : test, configFiles : /users/k19022845/.nextflow/assets/nf-core/nanoseq/nextflow.config Input/output options input : https://raw.githubusercontent.com/nf-core/test-datasets/nanoseq/3.0/samplesheet/samplesheet_nobc_dx.csv protocol : DNA outdir : ./results Demultiplexing options input_path : https://raw.githubusercontent.com/nf-core/test-datasets/nanoseq/fastq/nondemultiplexed/sample_nobc_dx.fastq.gz barcode_kit : NBD103/NBD104 Differential analysis options skip_quantification : true RNA fusion analysis options jaffal_ref_dir : null skip_fusion_analysis : true RNA modification analysis options skip_modification_analysis: true Process skipping options skip_bigbed : true skip_bigwig : true Reference genome options igenomes_base : s3://ngi-igenomes/igenomes/ Institutional config options config_profile_name : Test profile config_profile_description: Minimal test dataset to check pipeline function Max job request options max_cpus : 2 max_memory : 6 GB max_time : 12h !! Only displaying parameters that differ from the pipeline defaults !! ------------------------------------------------------ If you use nf-core/nanoseq for your analysis please cite: * The pipeline https://doi.org/10.5281/zenodo.5740870 * The nf-core framework https://doi.org/10.1038/s41587-020-0439-x * Software dependencies https://github.com/nf-core/nanoseq/blob/master/CITATIONS.md ------------------------------------------------------ executor > local (2) [8c/a34516] process > NFCORE_NANOSEQ:NANOSEQ:INPUT_CHECK:SAMPLESHEET_CHECK (samplesheet_nobc_dx.csv) [ 0%] 0 of 1 [d4/80e29c] process > NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz) [ 0%] 0 of 1 [- ] process > NFCORE_NANOSEQ:NANOSEQ:QCFASTQ_NANOPLOT_FASTQC:NANOPLOT - [- ] process > NFCORE_NANOSEQ:NANOSEQ:QCFASTQ_NANOPLOT_FASTQC:FASTQC - [- ] process > NFCORE_NANOSEQ:NANOSEQ:PREPARE_GENOME:GET_CHROM_SIZES - [- ] process > NFCORE_NANOSEQ:NANOSEQ:PREPARE_GENOME:GTF2BED - [- ] process > NFCORE_NANOSEQ:NANOSEQ:PREPARE_GENOME:SAMTOOLS_FAIDX - [- ] process > NFCORE_NANOSEQ:NANOSEQ:ALIGN_MINIMAP2:MINIMAP2_INDEX - [- ] process > NFCORE_NANOSEQ:NANOSEQ:ALIGN_MINIMAP2:MINIMAP2_ALIGN - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:SAMTOOLS_VIEW_BAM - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:SAMTOOLS_SORT - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:SAMTOOLS_INDEX - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_STATS - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_FLAGSTAT - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_IDXSTATS - [- ] process > NFCORE_NANOSEQ:NANOSEQ:CUSTOM_DUMPSOFTWAREVERSIONS - [- ] process > NFCORE_NANOSEQ:NANOSEQ:MULTIQC - Error executing process > 'NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz)' Caused by: Process `NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz)` terminated with an error exit status (127) Command executed: ## Unzip fastq file ## qcat doesnt support zipped files yet FILE=sample_nobc_dx.fastq.gz if [[ $FILE == *.gz ]] then zcat sample_nobc_dx.fastq.gz > unzipped.fastq FILE=unzipped.fastq fi qcat \ -f $FILE \ -b ./fastq \ --kit NBD103/NBD104 \ --min-score 60 \ ## Zip fastq files (cannot find pigz command) gzip fastq/* executor > local (2) [8c/a34516] process > NFCORE_NANOSEQ:NANOSEQ:INPUT_CHECK:SAMPLESHEET_CHECK (samplesheet_nobc_dx.csv) [ 0%] 0 of 1 [d4/80e29c] process > NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz) [100%] 1 of 1, failed: 1 ✘ [- ] process > NFCORE_NANOSEQ:NANOSEQ:QCFASTQ_NANOPLOT_FASTQC:NANOPLOT - [- ] process > NFCORE_NANOSEQ:NANOSEQ:QCFASTQ_NANOPLOT_FASTQC:FASTQC - [- ] process > NFCORE_NANOSEQ:NANOSEQ:PREPARE_GENOME:GET_CHROM_SIZES - [- ] process > NFCORE_NANOSEQ:NANOSEQ:PREPARE_GENOME:GTF2BED - [- ] process > NFCORE_NANOSEQ:NANOSEQ:PREPARE_GENOME:SAMTOOLS_FAIDX - [- ] process > NFCORE_NANOSEQ:NANOSEQ:ALIGN_MINIMAP2:MINIMAP2_INDEX - [- ] process > NFCORE_NANOSEQ:NANOSEQ:ALIGN_MINIMAP2:MINIMAP2_ALIGN - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:SAMTOOLS_VIEW_BAM - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:SAMTOOLS_SORT - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:SAMTOOLS_INDEX - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_STATS - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_FLAGSTAT - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_IDXSTATS - [- ] process > NFCORE_NANOSEQ:NANOSEQ:CUSTOM_DUMPSOFTWAREVERSIONS - [- ] process > NFCORE_NANOSEQ:NANOSEQ:MULTIQC - Execution cancelled -- Finishing pending tasks before exit Error executing process > 'NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz)' Caused by: Process `NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz)` terminated with an error exit status (127) Command executed: ## Unzip fastq file ## qcat doesnt support zipped files yet FILE=sample_nobc_dx.fastq.gz if [[ $FILE == *.gz ]] then zcat sample_nobc_dx.fastq.gz > unzipped.fastq FILE=unzipped.fastq fi qcat \ -f $FILE \ -b ./fastq \ --kit NBD103/NBD104 \ --min-score 60 \ ## Zip fastq files (cannot find pigz command) gzip fastq/* executor > local (2) [8c/a34516] process > NFCORE_NANOSEQ:NANOSEQ:INPUT_CHECK:SAMPLESHEET_CHECK (samplesheet_nobc_dx.csv) [100%] 1 of 1 ✔ [d4/80e29c] process > NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz) [100%] 1 of 1, failed: 1 ✘ [- ] process > NFCORE_NANOSEQ:NANOSEQ:QCFASTQ_NANOPLOT_FASTQC:NANOPLOT - [- ] process > NFCORE_NANOSEQ:NANOSEQ:QCFASTQ_NANOPLOT_FASTQC:FASTQC - [- ] process > NFCORE_NANOSEQ:NANOSEQ:PREPARE_GENOME:GET_CHROM_SIZES - [- ] process > NFCORE_NANOSEQ:NANOSEQ:PREPARE_GENOME:GTF2BED - [- ] process > NFCORE_NANOSEQ:NANOSEQ:PREPARE_GENOME:SAMTOOLS_FAIDX - [- ] process > NFCORE_NANOSEQ:NANOSEQ:ALIGN_MINIMAP2:MINIMAP2_INDEX - [- ] process > NFCORE_NANOSEQ:NANOSEQ:ALIGN_MINIMAP2:MINIMAP2_ALIGN - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:SAMTOOLS_VIEW_BAM - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:SAMTOOLS_SORT - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:SAMTOOLS_INDEX - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_STATS - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_FLAGSTAT - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_IDXSTATS - [- ] process > NFCORE_NANOSEQ:NANOSEQ:CUSTOM_DUMPSOFTWAREVERSIONS - [- ] process > NFCORE_NANOSEQ:NANOSEQ:MULTIQC - Execution cancelled -- Finishing pending tasks before exit -[nf-core/nanoseq] Pipeline completed with errors- Error executing process > 'NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz)' Caused by: Process `NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz)` terminated with an error exit status (127) Command executed: ## Unzip fastq file ## qcat doesnt support zipped files yet FILE=sample_nobc_dx.fastq.gz if [[ $FILE == *.gz ]] then zcat sample_nobc_dx.fastq.gz > unzipped.fastq FILE=unzipped.fastq fi qcat \ -f $FILE \ -b ./fastq \ --kit NBD103/NBD104 \ --min-score 60 \ ## Zip fastq files (cannot find pigz command) gzip fastq/* executor > local (2) [8c/a34516] process > NFCORE_NANOSEQ:NANOSEQ:INPUT_CHECK:SAMPLESHEET_CHECK (samplesheet_nobc_dx.csv) [100%] 1 of 1 ✔ [d4/80e29c] process > NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz) [100%] 1 of 1, failed: 1 ✘ [- ] process > NFCORE_NANOSEQ:NANOSEQ:QCFASTQ_NANOPLOT_FASTQC:NANOPLOT - [- ] process > NFCORE_NANOSEQ:NANOSEQ:QCFASTQ_NANOPLOT_FASTQC:FASTQC - [- ] process > NFCORE_NANOSEQ:NANOSEQ:PREPARE_GENOME:GET_CHROM_SIZES - [- ] process > NFCORE_NANOSEQ:NANOSEQ:PREPARE_GENOME:GTF2BED - [- ] process > NFCORE_NANOSEQ:NANOSEQ:PREPARE_GENOME:SAMTOOLS_FAIDX - [- ] process > NFCORE_NANOSEQ:NANOSEQ:ALIGN_MINIMAP2:MINIMAP2_INDEX - [- ] process > NFCORE_NANOSEQ:NANOSEQ:ALIGN_MINIMAP2:MINIMAP2_ALIGN - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:SAMTOOLS_VIEW_BAM - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:SAMTOOLS_SORT - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:SAMTOOLS_INDEX - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_STATS - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_FLAGSTAT - [- ] process > NFCORE_NANOSEQ:NANOSEQ:BAM_SORT_INDEX_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_IDXSTATS - [- ] process > NFCORE_NANOSEQ:NANOSEQ:CUSTOM_DUMPSOFTWAREVERSIONS - [- ] process > NFCORE_NANOSEQ:NANOSEQ:MULTIQC - Execution cancelled -- Finishing pending tasks before exit -[nf-core/nanoseq] Pipeline completed with errors- Error executing process > 'NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz)' Caused by: Process `NFCORE_NANOSEQ:NANOSEQ:QCAT (sample_nobc_dx.fastq.gz)` terminated with an error exit status (127) Command executed: ## Unzip fastq file ## qcat doesnt support zipped files yet FILE=sample_nobc_dx.fastq.gz if [[ $FILE == *.gz ]] then zcat sample_nobc_dx.fastq.gz > unzipped.fastq FILE=unzipped.fastq fi qcat \ -f $FILE \ -b ./fastq \ --kit NBD103/NBD104 \ --min-score 60 \ ## Zip fastq files (cannot find pigz command) gzip fastq/* cat <<-END_VERSIONS > versions.yml "NFCORE_NANOSEQ:NANOSEQ:QCAT": qcat: $(qcat --version 2>&1 | sed 's/^.*qcat //; s/ .*$//') END_VERSIONS Command exit status: 127 Command output: (empty) Command error: .command.sh: line 11: qcat: command not found Work dir: /scratch/prj/ppn_microglia_mod/directrna/scripts/work/d4/80e29c7e90053a9789ef55a7104488 Tip: view the complete command output by changing to the process work dir and entering the command `cat .command.out`
No response
Nextflow version: 22.10.1 Hardware: HPC Executor: local Container engine: singularity OS: Linux Version of nf-core/nanoseq: v3.1.0-g6e563e5
The text was updated successfully, but these errors were encountered:
Hi @rugilemat,
I think this is caused by the space between test, and singularity. Please try running the following instead:
test,
singularity
nextflow run nf-core/nanoseq -profile test,singularity
Thanks!
Best wishes, Yuk Kei
Sorry, something went wrong.
Hi @yuukiiwa, it seems to have worked without the space! Thank you!
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Description of the bug
Hi,
I have tried to install and run nanoseq on our HPC and got the following error when trying to run the test:
Any help would be appreciated!
Command used and terminal output
Relevant files
No response
System information
Nextflow version: 22.10.1
Hardware: HPC
Executor: local
Container engine: singularity
OS: Linux
Version of nf-core/nanoseq: v3.1.0-g6e563e5
The text was updated successfully, but these errors were encountered: