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From what I understood from the error messages the maximum input length of this pipeline is at 650 bases per read.
For reads longer 650 the RNA sequence seems to be cropped to a length of 650, while the quality string doesn't, leading to inequal quality string and sequence length.
Command used and terminal output
nextflow run /nfs/data3/CIRCEST/pipeline -profile apptainer,cluster -params-file ./configs/params.yamlPARAMS:input: './samplesheet.csv'outdir: './results/'save_reference: truesave_intermediates: truehisat2_build_memory: '200.GB'genome: 'WBcel235'star: nullmodule: 'circrna_discovery'ERROR ~ Error executing process > 'NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:STAR_1ST_PASS (elegans_unselected_1)'Caused by: Process `NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:STAR_1ST_PASS (elegans_unselected_1)` terminated with an error exit status (104)Command executed: STAR \ --genomeDir star \ --readFilesIn input1/elegans_unselected_1_trimmed.fq.gz \ --runThreadN 24 \ --outFileNamePrefix elegans_unselected_1. \ --outSAMtype BAM Unsorted \ \ --outSAMattrRGline 'ID:elegans_unselected_1' 'SM:elegans_unselected_1' \ --chimOutType Junctions WithinBAM --outSAMunmapped Within --outFilterType BySJout --outReadsUnmapped None --readFilesCommand zcat --alignSJDBoverhangMin 10 --chimJunctionOverhangMin 10 --chimSegmentMin 10 if [ -f elegans_unselected_1.Unmapped.out.mate1 ]; then mv elegans_unselected_1.Unmapped.out.mate1 elegans_unselected_1.unmapped_1.fastq gzip elegans_unselected_1.unmapped_1.fastq fi if [ -f elegans_unselected_1.Unmapped.out.mate2 ]; then mv elegans_unselected_1.Unmapped.out.mate2 elegans_unselected_1.unmapped_2.fastq gzip elegans_unselected_1.unmapped_2.fastq fi cat <<-END_VERSIONS > versions.yml "NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:STAR_1ST_PASS":executor > slurm (7)[54/b6824f] process > NFCORE_CIRCRNA:CIRCRNA:INPUT_CHECK:SAMPLESHEET_CHECK (samplesheet.csv) [100%] 1 of 1 ✔[- ] process > NFCORE_CIRCRNA:CIRCRNA:CAT_FASTQ -[- ] process > NFCORE_CIRCRNA:CIRCRNA:PREPARE_GENOME:BOWTIE_BUILD -[- ] process > NFCORE_CIRCRNA:CIRCRNA:PREPARE_GENOME:BOWTIE2_BUILD -[- ] process > NFCORE_CIRCRNA:CIRCRNA:PREPARE_GENOME:BWA_INDEX -[- ] process > NFCORE_CIRCRNA:CIRCRNA:PREPARE_GENOME:HISAT2_EXTRACTSPLICESITES -[- ] process > NFCORE_CIRCRNA:CIRCRNA:PREPARE_GENOME:HISAT2_BUILD -[5b/f8b873] process > NFCORE_CIRCRNA:CIRCRNA:PREPARE_GENOME:STAR_GENOMEGENERATE (genome.fa) [100%] 1 of 1 ✔[- ] process > NFCORE_CIRCRNA:CIRCRNA:PREPARE_GENOME:SEGEMEHL_INDEX -[00/9b89ee] process > NFCORE_CIRCRNA:CIRCRNA:FASTQC_TRIMGALORE:FASTQC (elegans_unselected_1) [100%] 1 of 1 ✔[95/3c54c8] process > NFCORE_CIRCRNA:CIRCRNA:FASTQC_TRIMGALORE:TRIMGALORE (elegans_unselected_1) [100%] 1 of 1 ✔[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:SEGEMEHL_ALIGN -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:SEGEMEHL_FILTER -[17/6ccdf3] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:STAR_1ST_PASS (elegans_unselected_1) [100%] 2 of 2, failed: 2..[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:STAR_SJDB -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:STAR_2ND_PASS -[39/0919bd] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:CIRCEXPLORER2_REF (genes.gtf) [100%] 1 of 1 ✔[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:CIRCEXPLORER2_PAR -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:CIRCEXPLORER2_ANN -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:CIRCEXPLORER2_FLT -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:CIRCRNA_FINDER_FILTER -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:FIND_CIRC_ALIGN -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:SAMTOOLS_INDEX -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:SAMTOOLS_VIEW -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:FIND_CIRC_ANCHORS -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:FIND_CIRC -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:FIND_CIRC_FILTER -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:CIRIQUANT_YML -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:CIRIQUANT -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:CIRIQUANT_FILTER -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:DCC_MATE1_1ST_PASS - [- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:DCC_MATE1_SJDB -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:DCC_MATE1_2ND_PASS -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:DCC_MATE2_1ST_PASS -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:DCC_MATE2_SJDB -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:DCC_MATE2_2ND_PASS -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:DCC -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:DCC_FILTER -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:MAPSPLICE_REFERENCE -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:MAPSPLICE_ALIGN -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:MAPSPLICE_PARSE -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:MAPSPLICE_ANNOTATE -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:MAPSPLICE_FILTER -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:COUNTS_SINGLE -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:REMOVE_HEADER -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:SPLIT_ANNOTATION -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:ANNOTATION -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:CAT_ANNOTATION -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:SORT_ANNOTATION -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:FASTA -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:PSIRC_INDEX -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:PSIRC_QUANT -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:PSIRC_COMBINE -[- ] process > NFCORE_CIRCRNA:CIRCRNA:MIRNA_PREDICTION:TARGETSCAN_DATABASE -[- ] process > NFCORE_CIRCRNA:CIRCRNA:MIRNA_PREDICTION:TARGETSCAN -[- ] process > NFCORE_CIRCRNA:CIRCRNA:MIRNA_PREDICTION:MIRANDA -[- ] process > NFCORE_CIRCRNA:CIRCRNA:MIRNA_PREDICTION:MIRNA_TARGETS -[- ] process > NFCORE_CIRCRNA:CIRCRNA:DIFFERENTIAL_EXPRESSION:HISAT2_ALIGN -[- ] process > NFCORE_CIRCRNA:CIRCRNA:DIFFERENTIAL_EXPRESSION:BAM_SORT_STATS_SAMTOOLS:SAMTOOLS_SORT -[- ] process > NFCORE_CIRCRNA:CIRCRNA:DIFFERENTIAL_EXPRESSION:BAM_SORT_STATS_SAMTOOLS:SAMTOOLS_INDEX -[- ] process > NFCORE_CIRCRNA:CIRCRNA:DIFFERENTIAL_EXPRESSION:BAM_SORT_STATS_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_STATS -[- ] process > NFCORE_CIRCRNA:CIRCRNA:DIFFERENTIAL_EXPRESSION:BAM_SORT_STATS_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_FLAG... -[- ] process > NFCORE_CIRCRNA:CIRCRNA:DIFFERENTIAL_EXPRESSION:BAM_SORT_STATS_SAMTOOLS:BAM_STATS_SAMTOOLS:SAMTOOLS_IDXS... -[- ] process > NFCORE_CIRCRNA:CIRCRNA:DIFFERENTIAL_EXPRESSION:STRINGTIE_STRINGTIE -[- ] process > NFCORE_CIRCRNA:CIRCRNA:DIFFERENTIAL_EXPRESSION:STRINGTIE_PREPDE -[- ] process > NFCORE_CIRCRNA:CIRCRNA:DIFFERENTIAL_EXPRESSION:DESEQ2_DIFFERENTIAL_EXPRESSION -[- ] process > NFCORE_CIRCRNA:CIRCRNA:DIFFERENTIAL_EXPRESSION:PARENT_GENE -[- ] process > NFCORE_CIRCRNA:CIRCRNA:DIFFERENTIAL_EXPRESSION:PREPARE_CLR_TEST -[- ] process > NFCORE_CIRCRNA:CIRCRNA:DIFFERENTIAL_EXPRESSION:CIRCTEST -[- ] process > NFCORE_CIRCRNA:CIRCRNA:CUSTOM_DUMPSOFTWAREVERSIONS -[- ] process > NFCORE_CIRCRNA:CIRCRNA:MULTIQC -ERROR ~ Error executing process > 'NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:STAR_1ST_PASS (elegans_unselected_1)'Caused by: Process `NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:STAR_1ST_PASS (elegans_unselected_1)` terminated with an error exit status (104)Command executed: STAR \ --genomeDir star \ --readFilesIn input1/elegans_unselected_1_trimmed.fq.gz \ --runThreadN 24 \ --outFileNamePrefix elegans_unselected_1. \ --outSAMtype BAM Unsorted \ \ --outSAMattrRGline 'ID:elegans_unselected_1' 'SM:elegans_unselected_1' \ --chimOutType Junctions WithinBAM --outSAMunmapped Within --outFilterType BySJout --outReadsUnmapped None --readFilesCommand zcat --alignSJDBoverhangMin 10 --chimJunctionOverhangMin 10 --chimSegmentMin 10 if [ -f elegans_unselected_1.Unmapped.out.mate1 ]; then mv elegans_unselected_1.Unmapped.out.mate1 elegans_unselected_1.unmapped_1.fastq gzip elegans_unselected_1.unmapped_1.fastq fi if [ -f elegans_unselected_1.Unmapped.out.mate2 ]; then mv elegans_unselected_1.Unmapped.out.mate2 elegans_unselected_1.unmapped_2.fastq gzip elegans_unselected_1.unmapped_2.fastq fi cat <<-END_VERSIONS > versions.yml "NFCORE_CIRCRNA:CIRCRNA:CIRCRNA_DISCOVERY:STAR_1ST_PASS": star: $(STAR --version | sed -e "s/STAR_//g") samtools: $(echo $(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*$//') gawk: $(echo $(gawk --version 2>&1) | sed 's/^.*GNU Awk //; s/, .*$//') END_VERSIONSCommand exit status: 104Command output: STAR --genomeDir star --readFilesIn input1/elegans_unselected_1_trimmed.fq.gz --runThreadN 24 --outFileNamePrefix elegans_unselected_1. --outSAMtype BAM Unsorted --outSAMattrRGline ID:elegans_unselected_1 SM:elegans_unselected_1 --chimOutType Junctions WithinBAM --outSAMunmapped Within --outFilterType BySJout --outReadsUnmapped None --readFilesCommand zcat --alignSJDBoverhangMin 10 --chimJunctionOverhangMin 10 --chimSegmentMin 10 STAR version: 2.7.9a compiled: 2021-05-04T09:43:56-0400 vega:/home/dobin/data/STAR/STARcode/STAR.master/source Nov 23 14:00:32 ..... started STAR run Nov 23 14:00:32 ..... loading genome Nov 23 14:00:34 ..... started mappingCommand error: EXITING because of FATAL ERROR in reads input: quality string length is not equal to sequence length @SRR19055922.2.1 AGAATTGGCTCTAGAGAATGCAGATATCATTGAGGTCGAGACCAAAAAGCCTTACAAGACTAAAGAATAAGAAAAACTGTTTTCACAGCAATAACAGAATTGAAAAGATCCATGATTACGCACCTCACTGGTCTCGAGAATGTCATGCAAGAGCTTTCTCTGTCAAGATAACTTGAAAGAGGTTCCATTCCTCAGCTTTCGCTGGACTCAAGTGCTCAACATTCCAGCCAAATGCAACAAAATCGAAAACATCCACCAAGGCTTTGTCAACATGACTTCCCTCATCGATGTCAACTTGGGATGCAATCAAATCAGCATGGCAGCTGATACTTTCGCCAACGTTCAAGATGTCTCCAGAACTTGATTCTTGATAATAACTGCATGACTGAATTCCCAAGCAAAGCTGTGAGAAACATGAACAACTTGATTGCTCTCAAATATAACAAGATCAACGCCATTAGACAAACGACTTTGTTAACCTCTCCTCCCTCTCCATGCTCTTAATGGAAACATTTTCTTGGCTTTAAAGGAGGAGCCCTCCAGAACCATCCAAATCTTCATATCTGTATTTGAATCAGGAACAATCTGCAAACTCGACAACGGAGTCTTGGAGCAATCAAGCAACTCCTGAGGTTTCGATCTATCTTCAA SOLUTION: fix your fastq file Nov 23 14:00:36 ...... FATAL ERROR, exitingWork dir: /nfs/data3/CIRCEST/runs/benchmarking/work/17/6ccdf33d1780d19e7b6bbe0973cdf6Tip: you can replicate the issue by changing to the process work dir and entering the command `bash .command.run` -- Check '.nextflow.log' file for details-[nf-core/circrna] Pipeline completed with errors-### Relevant files### System information_No response_
The text was updated successfully, but these errors were encountered:
Fabian-Boehm
changed the title
Incorrect fastq reading leads to different sequence and quality string lengths.
Limitted input length and inequal quality string lenths.
Nov 24, 2023
Fabian-Boehm
changed the title
Limitted input length and inequal quality string lenths.
Limitted input length.
Nov 24, 2023
Hey,
the cropping is probably only done in the error message, I can hardly imagine STAR doing something as substantial as this without giving a warning at least.
For the length inequality problem there are some related issues - maybe one of them applies to your data:
###Description of the bug
From what I understood from the error messages the maximum input length of this pipeline is at 650 bases per read.
For reads longer 650 the RNA sequence seems to be cropped to a length of 650, while the quality string doesn't, leading to inequal quality string and sequence length.
Command used and terminal output
The text was updated successfully, but these errors were encountered: