`NFCORE_RNASEQ:RNASEQ:FASTQ_ALIGN_HISAT2:HISAT2_ALIGN (pituitary_stage3-1)` terminated with an error exit status (1)
Description of the bug
running rnaseq-pipeline locally and I'm having trouble with fail to read the header from "-".
Command used and terminal output
# my cmd
nextflow run -qs 8 -profile singularity -bg /home/huyan/software/nf-core/rnaseq/nf-core-rnaseq_3.14.0/3_14_0/ --email [email protected] --input ./samplesheet.csv --fasta aaa_genomic.fna --gtf aaa_genomic.gtf --aligner hisat2 --skip_qualimap --save_reference --outdir ./00_test --max_memory 40.GB --max_cpus 8
# my error report
nf-core/rnaseq execution completed unsuccessfully!
The exit status of the task that caused the workflow execution to fail was: 1.
The full error message was:
Error executing process > 'NFCORE_RNASEQ:RNASEQ:FASTQ_ALIGN_HISAT2:HISAT2_ALIGN (pituitary_stage3-1)'
Caused by:
Process `NFCORE_RNASEQ:RNASEQ:FASTQ_ALIGN_HISAT2:HISAT2_ALIGN (pituitary_stage3-1)` terminated with an error exit status (1)
Command executed:
INDEX=`find -L ./ -name "*.1.ht2" | sed 's/\.1.ht2$//'`
hisat2 \
-x $INDEX \
-1 pituitary_stage3-1_1_val_1.fq.gz \
-2 pituitary_stage3-1_2_val_2.fq.gz \
\
--known-splicesite-infile aaa_genomic.filtered.splice_sites.txt \
--summary-file pituitary_stage3-1.hisat2.summary.log \
--threads 8 \
--rg-id pituitary_stage3-1 --rg SM:pituitary_stage3-1 \
\
--no-mixed \
--no-discordant \
--met-stderr --new-summary --dta \
| samtools view -bS -F 4 -F 8 -F 256 - > pituitary_stage3-1.bam
if [ -f pituitary_stage3-1.unmapped.fastq.1.gz ]; then
mv pituitary_stage3-1.unmapped.fastq.1.gz pituitary_stage3-1.unmapped_1.fastq.gz
fi
if [ -f pituitary_stage3-1.unmapped.fastq.2.gz ]; then
mv pituitary_stage3-1.unmapped.fastq.2.gz pituitary_stage3-1.unmapped_2.fastq.gz
fi
cat <<-END_VERSIONS > versions.yml
"NFCORE_RNASEQ:RNASEQ:FASTQ_ALIGN_HISAT2:HISAT2_ALIGN":
hisat2: 2.2.1
samtools: $(echo $(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*$//')
END_VERSIONS
Command exit status:
1
Command output:
(empty)
Command error:
WARNING: Skipping mount /usr/local/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container
(ERR): mkfifo(/tmp/53.inpipe1) failed.
Exiting now ...
[main_samview] fail to read the header from "-".
Work dir:
~/project/work/f2/3c12bc9bf0e4ae9ae09f6ca2a68a96
Tip: when you have fixed the problem you can continue the execution adding the option `-resume` to the run command line
Relevant files
more detail
https://github.com/nf-core/rnaseq/issues/1092#issuecomment-2002547658
System information
No response
Same issue here. Did you find a solution?
It seems that there is a memory allocation issue with HiSAT2 aligner . Modify your config file based on the CPU and memory availability:
process { executor = ‘local’ }
params { max_cpus = 24 max_memory = 500.GB max_time = 400.h }
Seems to be a duplicate of https://github.com/nf-core/rnaseq/issues/1288
I still have same problem. Increasing the memory size did not solve the issue!!!