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Description
I'm running this pipeline in an HPC environment, but I'm getting an error where the container effectively can't be found.
The error appears to be looking for
community-cr-prod.seqera.io-docker-registry-v2-blobs-sha256-4a-4a1cddfad5b503ee347cc5de17d172e1876c547fca00aa844559c9e764fb400f-data.img
but the container that is present is
community-cr-prod.seqera.io-docker-registry-v2-blobs-sha256-45-4569ff9993578b8402d00230ab9dd75ce6e63529731eb24f21579845e6bd5cdb-data.img
This results in the step (and the whole workflow) failing. Any ideas?
In our HPC environment, the nf-core containers are located centrally, but manually downloading the containers locally via nf-core download pulls down an exactly matching container list, so I'm unable to find a container with the hash that matches the error. I tracked the reference down to
| 'https://community-cr-prod.seqera.io/docker/registry/v2/blobs/sha256/4a/4a1cddfad5b503ee347cc5de17d172e1876c547fca00aa844559c9e764fb400f/data' : |
$ nextflow run nf-core/chipseq -r 2.1.0 -profile singularity --input samples_GSM325933.csv --outdir results_GSM325933 --fasta chm13v2.0.fa --gtf chm13v2.0_RefSeq_Liftoff_v5.2.gtf --igenomes_ignore --genome null --aligner bowtie2 --macs_gsize 3117292070 --keep_multi_map --save_unaligned --narrow_peak --skip_preseq
Nextflow 24.10.3 is available - Please consider updating your version to it
N E X T F L O W ~ version 24.04.4
Launching `https://github.com/nf-core/chipseq` [cheeky_kirch] DSL2 - revision: 76e2382b6d [2.1.0]
WARN: Access to undefined parameter `monochromeLogs` -- Initialise it to a default value eg. `params.monochromeLogs = some_value`
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,--./,-.
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|\ | |__ __ / ` / \ |__) |__ } {
| \| | \__, \__/ | \ |___ \`-._,-`-,
`._,._,'
nf-core/chipseq v2.1.0-g76e2382
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Core Nextflow options
revision : 2.1.0
runName : cheeky_kirch
containerEngine: singularity
launchDir : /n/scratch/users/a/at237/kornelia
workDir : /n/scratch/users/a/at237/kornelia/work
projectDir : /home/at237/.nextflow/assets/nf-core/chipseq
userName : at237
profile : singularity
configFiles :
Input/output options
input : samples_GSM325933.csv
outdir : results_GSM325933
Reference genome options
genome : null
fasta : chm13v2.0.fa
gtf : chm13v2.0_RefSeq_Liftoff_v5.2.gtf
macs_gsize : 3117292070
igenomes_ignore: true
Alignment options
aligner : bowtie2
keep_multi_map : true
save_unaligned : true
Peak calling options
narrow_peak : true
Process skipping options
skip_preseq : true
!! Only displaying parameters that differ from the pipeline defaults !!
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If you use nf-core/chipseq for your analysis please cite:
* The pipeline
https://doi.org/10.5281/zenodo.3240506
* The nf-core framework
https://doi.org/10.1038/s41587-020-0439-x
* Software dependencies
https://github.com/nf-core/chipseq/blob/master/CITATIONS.md
------------------------------------------------------
executor > local (71)
[f1/2b2bdc] NFCORE_CHIPSEQ:PREPARE_GENOME:GTF2BED (chm13v2.0_RefSeq_Liftoff_v5.2.gtf) [100%] 1 of 1 ✔
[c4/f3b6f5] NFCORE_CHIPSEQ:PREPARE_GENOME:CUSTOM_GETCHROMSIZES (chm13v2.0.fa) [100%] 1 of 1 ✔
[7f/492eff] NFCORE_CHIPSEQ:PREPARE_GENOME:GENOME_BLACKLIST_REGIONS (chm13v2.0.fa.sizes) [100%] 1 of 1 ✔
[1a/5d4f5c] NFCORE_CHIPSEQ:PREPARE_GENOME:BOWTIE2_BUILD (chm13v2.0.fa) [100%] 1 of 1 ✔
[53/7c2254] NFCORE_CHIPSEQ:CHIPSEQ:INPUT_CHECK:SAMPLESHEET_CHECK (samples_GSM325933.csv) [100%] 1 of 1 ✔
[e9/b65e15] NFCORE_CHIPSEQ:CHIPSEQ:FASTQ_FASTQC_UMITOOLS_TRIMGALORE:FASTQC (Input_REP5_T1) [100%] 6 of 6 ✔
[e3/a3b565] NFCORE_CHIPSEQ:CHIPSEQ:FASTQ_FASTQC_UMITOOLS_TRIMGALORE:TRIMGALORE (Input_REP4_T1) [100%] 6 of 6 ✔
[ad/3e37bc] NFCORE_CHIPSEQ:CHIPSEQ:FASTQ_ALIGN_BOWTIE2:BOWTIE2_ALIGN (Input_REP4_T1) [100%] 6 of 6 ✔
executor > local (71)
[f1/2b2bdc] NFCORE_CHIPSEQ:PREPARE_GENOME:GTF2BED (chm13v2.0_RefSeq_Liftoff_v5.2.gtf) [100%] 1 of 1 ✔
[c4/f3b6f5] NFCORE_CHIPSEQ:PREPARE_GENOME:CUSTOM_GETCHROMSIZES (chm13v2.0.fa) [100%] 1 of 1 ✔
[7f/492eff] NFCORE_CHIPSEQ:PREPARE_GENOME:GENOME_BLACKLIST_REGIONS (chm13v2.0.fa.sizes) [100%] 1 of 1 ✔
[1a/5d4f5c] NFCORE_CHIPSEQ:PREPARE_GENOME:BOWTIE2_BUILD (chm13v2.0.fa) [100%] 1 of 1 ✔
[53/7c2254] NFCORE_CHIPSEQ:CHIPSEQ:INPUT_CHECK:SAMPLESHEET_CHECK (samples_GSM325933.csv) [100%] 1 of 1 ✔
[e9/b65e15] NFCORE_CHIPSEQ:CHIPSEQ:FASTQ_FASTQC_UMITOOLS_TRIMGALORE:FASTQC (Input_REP5_T1) [100%] 6 of 6 ✔
[e3/a3b565] NFCORE_CHIPSEQ:CHIPSEQ:FASTQ_FASTQC_UMITOOLS_TRIMGALORE:TRIMGALORE (Input_REP4_T1) [100%] 6 of 6 ✔
[ad/3e37bc] NFCORE_CHIPSEQ:CHIPSEQ:FASTQ_ALIGN_BOWTIE2:BOWTIE2_ALIGN (Input_REP4_T1) [100%] 6 of 6 ✔
[30/739122] NFCORE_CHIPSEQ:CHIPSEQ:FASTQ_ALIGN_BOWTIE2:BAM_SORT_STATS_SAMTOOLS:SAMTOOLS_SORT (Input_REP4_T1) [100%] 6 of 6 ✔
[d9/2509dc] NFCORE_CHIPSEQ:CHIPSEQ:FASTQ_ALIGN_BOWTIE2:BAM_SORT_STATS_SAMTOOLS:SAMTOOLS_INDEX (Input_REP4_T1) [100%] 6 of 6 ✔
[ad/f4ce45] NFC…STQ_ALIGN_BOWTIE2:BAM_SORT_STATS_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_STATS (PolII_K562_REP1_T1) [100%] 6 of 6 ✔
[89/c5273e] NFC…_ALIGN_BOWTIE2:BAM_SORT_STATS_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_FLAGSTAT (PolII_K562_REP1_T1) [100%] 6 of 6 ✔
[8f/edbae5] NFC…_ALIGN_BOWTIE2:BAM_SORT_STATS_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_IDXSTATS (PolII_K562_REP1_T1) [100%] 6 of 6 ✔
[98/fecf4a] NFCORE_CHIPSEQ:CHIPSEQ:PICARD_MERGESAMFILES (Input_REP4) [100%] 6 of 6 ✔
[ef/fe53e0] NFCORE_CHIPSEQ:CHIPSEQ:BAM_MARKDUPLICATES_PICARD:PICARD_MARKDUPLICATES (Input_REP2) [ 66%] 4 of 6
[20/dfc110] NFCORE_CHIPSEQ:CHIPSEQ:BAM_MARKDUPLICATES_PICARD:SAMTOOLS_INDEX (Input_REP2) [100%] 4 of 4
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_MARKDUPLICATES_PICARD:BAM_STATS_SAMTOOLS:SAMTOOLS_STATS -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_MARKDUPLICATES_PICARD:BAM_STATS_SAMTOOLS:SAMTOOLS_FLAGSTAT -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_MARKDUPLICATES_PICARD:BAM_STATS_SAMTOOLS:SAMTOOLS_IDXSTATS -
[9d/9e801f] NFCORE_CHIPSEQ:CHIPSEQ:BAM_FILTER_BAMTOOLS:BAMTOOLS_FILTER (Input_REP5) [ 25%] 1 of 4
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_FILTER_BAMTOOLS:SAMTOOLS_INDEX [ 0%] 0 of 1
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_FILTER_BAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_STATS -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_FILTER_BAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_FLAGSTAT -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_FILTER_BAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_IDXSTATS -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_FILTER_BAMTOOLS:SAMTOOLS_SORT -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_FILTER_BAMTOOLS:BAM_REMOVE_ORPHANS -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_FILTER_BAMTOOLS:BAM_SORT_STATS_SAMTOOLS:SAMTOOLS_SORT -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_FILTER_BAMTOOLS:BAM_SORT_STATS_SAMTOOLS:SAMTOOLS_INDEX -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_FILTER_BAMTOOLS:BAM_SORT_STATS_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_STATS -
[- ] NFC…CHIPSEQ:CHIPSEQ:BAM_FILTER_BAMTOOLS:BAM_SORT_STATS_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_FLAGSTAT -
[- ] NFC…CHIPSEQ:CHIPSEQ:BAM_FILTER_BAMTOOLS:BAM_SORT_STATS_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_IDXSTATS -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:PICARD_COLLECTMULTIPLEMETRICS [ 0%] 0 of 1
[- ] NFCORE_CHIPSEQ:CHIPSEQ:PHANTOMPEAKQUALTOOLS -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:MULTIQC_CUSTOM_PHANTOMPEAKQUALTOOLS -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_BEDGRAPH_BIGWIG_BEDTOOLS_UCSC:BEDTOOLS_GENOMECOV -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:BAM_BEDGRAPH_BIGWIG_BEDTOOLS_UCSC:UCSC_BEDGRAPHTOBIGWIG -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:DEEPTOOLS_COMPUTEMATRIX -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:DEEPTOOLS_PLOTPROFILE -
[- ] NFCORE_CHIPSEQ:CHIPSEQ:DEEPTOOLS_PLOTHEATMAP -
Plus 14 more processes waiting for tasks…
ERROR ~ Error executing process > 'NFCORE_CHIPSEQ:CHIPSEQ:PHANTOMPEAKQUALTOOLS (1)'
Caused by:
java.io.FileNotFoundException: /n/app/singularity/containers/nf-core/chipseq/2.1.0/.community-cr-prod.seqera.io-docker-registry-v2-blobs-sha256-4a-4a1cddfad5b503ee347cc5de17d172e1876c547fca00aa844559c9e764fb400f-data.img.lock (Permission denied)
-- Check '.nextflow.log' file for details
ERROR ~ Pipeline failed. Please refer to troubleshooting docs: https://nf-co.re/docs/usage/troubleshooting
-- Check '.nextflow.log' file for details
-[nf-core/chipseq] Pipeline completed with errors-
WARN: Killing running tasks (3)