rnasplice
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Exception: Event ENSG00000004961 not found in pickled directory index. Are you sure this is the right directory for the event?
Description of the bug
This issue appears in various forms in other issues, but I could not find a workable solution. This error occurs when running the pipeline with --genome GRCh38
or with manually provided --fasta
and --gtf
(I use those from 10x Genomics).
-[nf-core/rnasplice] Pipeline completed with errors-
ERROR ~ Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI (1)'
Caused by:
Process `NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI (1)` terminated with an error exit status (1)
Command executed:
sashimi_plot --plot-event ENSG00000004961 index miso_settings.txt --output-dir sashimi
cat <<-END_VERSIONS > versions.yml
"NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI":
python: $(python --version | sed "s/Python //g")
misopy: $(python -c "import pkg_resources; print(pkg_resources.get_distribution('misopy').version)")
END_VERSIONS
Command exit status:
1
Command output:
(empty)
Command error:
INFO: Converting SIF file to temporary sandbox...
/usr/local/lib/python2.7/site-packages/matplotlib/cbook/deprecation.py:107: MatplotlibDeprecationWarning: The mpl_toolkits.axes_grid module was deprecated in version 2.1. Use mpl_toolkits.axes_grid1 and mpl_toolkits.axisartist provies the same functionality instead.
warnings.warn(message, mplDeprecation, stacklevel=1)
Traceback (most recent call last):
File "/usr/local/bin/sashimi_plot", line 11, in <module>
sys.exit(main())
File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/sashimi_plot.py", line 276, in main
plot_label=plot_label)
File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/sashimi_plot.py", line 142, in plot_event
%(event_name, pickle_dir)
Exception: Event ENSG00000004961 not found in pickled directory index. Are you sure this is the right directory for the event?
INFO: Cleaning up image...
Work dir:
/lustre/home/mdozmorov/data/WorkData/Tony/Krista/RPE1_GFP_MYCN_DAC_72hrs/work/fe/1da2e608fc7aac0f8f63541f62c08b
A workaround is to set --sashimi_plot false
. But is there a better solution?
Command used and terminal output
export NXF_OPTS='-Xms8g -Xmx24g'
export NXF_SINGULARITY_CACHEDIR=/lustre/home/mdozmorov/singularity_cache
DIRIN=/lustre/home/mdozmorov/data/WorkData/
INPUT=${DIRIN}/samplesheet.csv
DIROUT=${DIRIN}/OUT_full
GENOME=/lustre/home/mdozmorov/data/ExtData/10x/refdata-gex-GRCh38-2024-A/fasta/genome.fa
GTF=/lustre/home/mdozmorov/data/ExtData/10x/refdata-gex-GRCh38-2024-A/genes/genes.gtf
nextflow run nf-core/rnasplice \
--input ${INPUT} \
--contrasts contrastsheet.csv \
--fasta ${GENOME} \
--gtf ${GTF} \
--outdir ${DIROUT} \
-profile singularity \
--sashimi_plot false \
-resume
Relevant files
No response
System information
nextflow version 23.10.0.5891, run on HPC in local mode, Singularity, Rocky Linux 9.4, nf-core/rnasplice: 1.0.4