The exit status of the task that caused the workflow execution to fail was: 255
.
The full error message was:
Error executing process > 'NFCORE_METHYLSEQ:METHYLSEQ:BISMARK:BISMARK_ALIGN (zr3644_6)' Caused by: Process `NFCORE_METHYLSEQ:METHYLSEQ:BISMARK:BISMARK_ALIGN (zr3644_6)` terminated with an error exit status (255) Command executed: ln -sf $(readlink GCF_963853765.1_xbMagGiga1.1_genomic.fa) BismarkIndex/GCF_963853765.1_xbMagGiga1.1_genomic.fa bismark \ -1 zr3644_6_R1_val_1_val_1_val_1.fq.gz -2 zr3644_6_R2_val_2_val_2_val_2.fq.gz \ --genome BismarkIndex \ --bam \ --score_min L,0,-0.8 --non_directional --prefix zr3644_6 --multicore 2 cat <<-END_VERSIONS > versions.yml "NFCORE_METHYLSEQ:METHYLSEQ:BISMARK:BISMARK_ALIGN": bismark: $(echo $(bismark -v 2>&1) | sed 's/^.*Bismark Version: v//; s/Copyright.*$//') END_VERSIONS Command exit status: 255 Command output: chr NC_088853.1 (76070991 bp) chr NC_088854.1 (61469542 bp) chr NC_088855.1 (61039741 bp) chr NC_088856.1 (57946171 bp) chr NC_088857.1 (57274926 bp) chr NC_088858.1 (56905015 bp) chr NC_088859.1 (53672946 bp) chr NC_088860.1 (51133819 bp) chr NC_088861.1 (50364239 bp) chr NC_088862.1 (37310742 bp) chr NW_027062568.1 (15579 bp) chr NW_027062569.1 (16498 bp) chr NW_027062570.1 (4000 bp) chr NW_027062571.1 (36893 bp) chr NW_027062572.1 (51000 bp) chr NW_027062573.1 (2000 bp) chr NW_027062574.1 (37061 bp) chr NW_027062575.1 (49428 bp) chr NW_027062576.1 (49232 bp) chr NW_027062577.1 (17087 bp) chr NW_027062578.1 (34507 bp) chr NW_027062579.1 (64000 bp) chr NW_027062580.1 (24229 bp) chr NW_027062581.1 (5000 bp) chr NW_027062582.1 (18808 bp) chr NW_027062583.1 (1000 bp) chr NW_027062584.1 (74000 bp) chr NW_027062585.1 (39334 bp) chr NW_027062586.1 (258015 bp) Command error: Found first alignment: A00742:173:HMGVGDSXY:2:1101:4128:1000_1:N:0:NATTAGTG+TATGTAGT/1 99 NC_088859.1_CT_converted 11770649 40 40M1D75M = 11770657 121 ATTTATTTAATATGTATAGAAATGTATATTTTATTGTGGTAAAAAAAATTTTATTATATATGTAAATGTATTTGTGGATAATTTGAAATGAATTAGTGTGTTGGAAGTTATTTGT FFFFFFFFFFFFFFF:F:FF,,:FFFF,F:::,,FF,FFF:,F:FFFFF,,F,F,FF:FFFFF,:F:F,,,,,F:FF,F,:FFFFF,:,FF,,,,F,F,,:FFF,,FF,,,F,F: AS:i:-20 XN:i:0 XM:i:2 XO:i:1 XG:i:1 NM:i:3 MD:Z:40^A14A44T15 YS:i:-26 YT:Z:CP A00742:173:HMGVGDSXY:2:1101:4128:1000_2:N:0:NATTAGTG+TATGTAGT/2 147 NC_088859.1_CT_converted 11770657 40 32M1D80M = 11770649 -121 AAGATGTATAGAAATGTATATTTGATTGTGGTAAAAAAAATTTTATAATATATGTAAATGTATGTGTGGATAATTTGAAATGAATTAGTGTTTTGGAAGTTATTTGTAATGG FF,F,F,:,,F,:,,FF,,:,:F,:,:F,FF,F,:FF,F:::::F,F:,,,:,F:,F,,F:F:,,F:FFF,F,F,:FFFF,F:,,,FFFFFF,:FF,,F,:::,,FFFF:FF AS:i:-26 XN:i:0 XM:i:3 XO:i:1 XG:i:1 NM:i:4 MD:Z:2T20T8^A31T48 YS:i:-20 YT:Z:CP Now starting a Bowtie 2 paired-end alignment for GAread1CTread2GAgenome (reading in sequences from zr3644_6.zr3644_6_R1_val_1_val_1_val_1.fq.gz.temp.2_G_to_A.fastq and zr3644_6.zr3644_6_R2_val_2_val_2_val_2.fq.gz.temp.2_C_to_T.fastq, with the options: -q --score-min L,0,-0.8 --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --norc)) Found first alignment: A00742:173:HMGVGDSXY:2:1101:1832:1000_1:N:0:NATTAGTG+TATGTAGT/1 83 NC_088856.1_CT_converted 13082717 2 20M2D15M1D70M1D4M1I5M = 13082695 -140 AAGGGTGATTTGGGAGTTATATTGTTTTTTATAGTAAAAAATTGTAATTTATGGTGTTAGTTTTGGATTGATTAATTTTATTTTTAAATATATTTTGTATAAATATTTGATTTTA FFF,F:FF,,::::FFF:FF,FFF:F,,F:F:F:FFFFFFFFFFFFFFFFFFFFFFF:FFFFFF:FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF AS:i:-89 XS:i:-77 XN:i:0 XM:i:9 XO:i:4 XG:i:5 NM:i:14 MD:Z:1T2A15^AG9G5^A51T3A6G0G0A5^G5A3 YS:i:-74 YT:Z:CP A00742:173:HMGVGDSXY:2:1101:1832:1000_2:N:0:NATTAGTG+TATGTAGT/2 163 NC_088856.1_CT_converted 13082695 2 18M1I1M2I23M2D15M1D54M = 13082717 140 TGGTTTTTGGTTTGAAAATATTTGGAAGGGTGATTTGGGAGTTATATTGTTTTTTATAGTAAAAAATTGTAATTTATGGTGTTAGTTTTGGATTGATTAATTTTATTTTTAAAT FFFFFFFFFFFFFFFFFFFFFFFF,FFFFFFFFFFFFFFFFFFFFFF,FFFFFFFFFFFFFFFFFFFF:FFFFFFFFFFFFF:FFFFFFFFFF:FFFFFFFFF:FFFFFFFFFF AS:i:-74 XS:i:-89 XN:i:0 XM:i:6 XO:i:4 XG:i:6 NM:i:12 MD:Z:0A0A21T2A15^AG9G5^A51T2 YS:i:-89 YT:Z:CP Now starting a Bowtie 2 paired-end alignment for CTread1GAread2GAgenome (reading in sequences from zr3644_6.zr3644_6_R1_val_1_val_1_val_1.fq.gz.temp.1_C_to_T.fastq and zr3644_6.zr3644_6_R2_val_2_val_2_val_2.fq.gz.temp.1_G_to_A.fastq, with the options: -q --score-min L,0,-0.8 --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --nofw)) Found first alignment: A00742:173:HMGVGDSXY:2:1101:4128:1000_1:N:0:NATTAGTG+TATGTAGT/1 77 * 0 0 * * 0 0 ATTTATTTAATATATATAAAAATATATATTTTATTATAATAAAAAAAATTTTATCATATATATAAATATATTTATAAATAATTTAAAATAAATTAATATATTAAAAATTATTTAT FFFFFFFFFFFFFFF:F:FF,,:FFFF,F:::,,FF,FFF:,F:FFFFF,,F,F,FF:FFFFF,:F:F,,,,,F:FF,F,:FFFFF,:,FF,,,,F,F,,:FFF,,FF,,,F,F: YT:Z:UP A00742:173:HMGVGDSXY:2:1101:4128:1000_2:N:0:NATTAGTG+TATGTAGT/2 141 * 0 0 * * 0 0 TTATTATAAATAATTTTTAAAATATTAATTTATTTTAAATTATTTATATATATATTTATATATATTATAAAATTTTTTTTATTATAATTAAATATATATTTTTATATATTTT FF:FFFF,,:::,F,,FF:,FFFFFF,,,:F,FFFF:,F,F,FFF:F,,:F:F,,F,:F,:,,,:F,F:::::F,FF:,F,FF,F:,:,F:,:,,FF,,:,F,,:,F,F,FF YT:Z:UP Now starting a Bowtie 2 paired-end alignment for GAread1CTread2CTgenome (reading in sequences from zr3644_6.zr3644_6_R1_val_1_val_1_val_1.fq.gz.temp.2_G_to_A.fastq and zr3644_6.zr3644_6_R2_val_2_val_2_val_2.fq.gz.temp.2_C_to_T.fastq, with the options: -q --score-min L,0,-0.8 --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --nofw)) Found first alignment: A00742:173:HMGVGDSXY:2:1101:1832:1000_1:N:0:NATTAGTG+TATGTAGT/1 77 * 0 0 * * 0 0 TAAAATTAAATATTTATATAAAATATATTTAAAAATAAAATTAATTAATTTAAAATTAATATTATAAATTATAATTTTTTATTATAAAAAATAATATAATTTTTAAATTATTTTT FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF:FFFFFF:FFFFFFFFFFFFFFFFFFFFFFF:F:F:F,,F:FFF,FF:FFF::::,,FF:F,FFF YT:Z:UP A00742:173:HMGVGDSXY:2:1101:1832:1000_2:N:0:NATTAGTG+TATGTAGT/2 141 * 0 0 * * 0 0 TAATTTTTAATTTAAAAATATTTAAAAAAATAATTTAAAAATTATATTATTTTTTATAATAAAAAATTATAATTTATAATATTAATTTTAAATTAATTAATTTTATTTTTAAAT FFFFFFFFFFFFFFFFFFFFFFFF,FFFFFFFFFFFFFFFFFFFFFF,FFFFFFFFFFFFFFFFFFFF:FFFFFFFFFFFFF:FFFFFFFFFF:FFFFFFFFF:FFFFFFFFFF YT:Z:UP >>> Writing bisulfite mapping results to zr3644_6.zr3644_6_R1_val_1_val_1_val_1.fq.gz.temp.1_bismark_bt2_pe.bam <<< Found first alignment: A00742:173:HMGVGDSXY:2:1101:4128:1000_1:N:0:NATTAGTG+TATGTAGT/1 77 * 0 0 * * 0 0 ATTTATTTAATATATATAAAAATATATATTTTATTATAATAAAAAAAATTTTATCATATATATAAATATATTTATAAATAATTTAAAATAAATTAATATATTAAAAATTATTTAT FFFFFFFFFFFFFFF:F:FF,,:FFFF,F:::,,FF,FFF:,F:FFFFF,,F,F,FF:FFFFF,:F:F,,,,,F:FF,F,:FFFFF,:,FF,,,,F,F,,:FFF,,FF,,,F,F: YT:Z:UP A00742:173:HMGVGDSXY:2:1101:4128:1000_2:N:0:NATTAGTG+TATGTAGT/2 141 * 0 0 * * 0 0 TTATTATAAATAATTTTTAAAATATTAATTTATTTTAAATTATTTATATATATATTTATATATATTATAAAATTTTTTTTATTATAATTAAATATATATTTTTATATATTTT FF:FFFF,,:::,F,,FF:,FFFFFF,,,:F,FFFF:,F,F,FFF:F,,:F:F,,F,:F,:,,,:F,F:::::F,FF:,F,FF,F:,:,F:,:,,FF,,:,F,,:,F,F,FF YT:Z:UP Now starting a Bowtie 2 paired-end alignment for CTread1GAread2GAgenome (reading in sequences from zr3644_6.zr3644_6_R1_val_1_val_1_val_1.fq.gz.temp.2_C_to_T.fastq and zr3644_6.zr3644_6_R2_val_2_val_2_val_2.fq.gz.temp.2_G_to_A.fastq, with the options: -q --score-min L,0,-0.8 --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --nofw)) Reading in the sequence files zr3644_6_R1_val_1_val_1_val_1.fq.gz.temp.1 and zr3644_6_R2_val_2_val_2_val_2.fq.gz.temp.1 Found first alignment: A00742:173:HMGVGDSXY:2:1101:4128:1000_1:N:0:NATTAGTG+TATGTAGT/1 77 * 0 0 * * 0 0 ATTTATTTAATATGTATAGAAATGTATATTTTATTGTGGTAAAAAAAATTTTATTATATATGTAAATGTATTTGTGGATAATTTGAAATGAATTAGTGTGTTGGAAGTTATTTGT FFFFFFFFFFFFFFF:F:FF,,:FFFF,F:::,,FF,FFF:,F:FFFFF,,F,F,FF:FFFFF,:F:F,,,,,F:FF,F,:FFFFF,:,FF,,,,F,F,,:FFF,,FF,,,F,F: YT:Z:UP A00742:173:HMGVGDSXY:2:1101:4128:1000_2:N:0:NATTAGTG+TATGTAGT/2 141 * 0 0 * * 0 0 CCATTACAAATAACTTCCAAAACACTAATTCATTTCAAATTATCCACACATACATTTACATATATTATAAAATTTTTTTTACCACAATCAAATATACATTTCTATACATCTT FF:FFFF,,:::,F,,FF:,FFFFFF,,,:F,FFFF:,F,F,FFF:F,,:F:F,,F,:F,:,,,:F,F:::::F,FF:,F,FF,F:,:,F:,:,,FF,,:,F,,:,F,F,FF YT:Z:UP >>> Writing bisulfite mapping results to zr3644_6.zr3644_6_R1_val_1_val_1_val_1.fq.gz.temp.2_bismark_bt2_pe.bam <<< Reading in the sequence files zr3644_6_R1_val_1_val_1_val_1.fq.gz.temp.2 and zr3644_6_R2_val_2_val_2_val_2.fq.gz.temp.2 Chromosomal sequence could not be extracted for A00742:173:HMGVGDSXY:2:1101:29767:30311_1:N:0:CATTAGTG+TATGTAGT NW_027062570.1 3928 Chromosomal sequence could not be extracted for A00742:173:HMGVGDSXY:2:1131:9173:2785_1:N:0:CATTAGTG+TATGTAGT NW_027062570.1 1 Processed 1000000 sequence pairs so far Processed 1000000 sequence pairs so far Processed 2000000 sequence pairs so far Processed 3000000 sequence pairs so far Processed 2000000 sequence pairs so far Chromosomal sequence could not be extracted for A00742:173:HMGVGDSXY:2:1237:21477:23187_1:N:0:CATTAGTG+TATGTAGT NW_027062570.1 3918 Processed 3000000 sequence pairs so far (ERR): bowtie2-align died with signal 9 (KILL) (ERR): bowtie2-align died with signal 9 (KILL) Use of uninitialized value $alignment_score_2 in concatenation (.) or string at /usr/local/bin/bismark line 3378,line 12676024. Use of uninitialized value $MD_tag_2 in concatenation (.) or string at /usr/local/bin/bismark line 3378, line 12676024. Failed to extract alignment score 2 () and MD tag ()! last alignment 1: A00742:173:HMGVGDSXY:2:1234:18611:21856_1:N:0:CATTAGTG+TATGTAGT/1 99 NC_088854.1_CT_converted 32160553 18 115M = 32160648 209 ATTAATAATATTATTTTATTGGTTAAGGATTTAAGGTTATTTTTGGTTTTTTAATGGATATTTTATTTAAGAGGATTTTTTGTATTTTTATAGTGGTTGAATTATGTTGAAGTTT FF:FFFFFFFFFF:FFFFFFFFFFFF:FFFFFFFFFFF:FFF:FFFFFFFFFFFFFFFFF:FF:FFFFFFFF:FFFF::FFFFFF:FFF:FFFFFF:FFFFFFFFFFFFFFFFFF AS:i:-6 XS:i:-26 XN:i:0 XM:i:1 XO:i:0 XG:i:0 NM:i:1 MD:Z:83T31 YS:i:-6 YT:Z:CP last alignment 2: A00742:173:HMGVGDSXY:2:1234:18611:21856_2:N:0:CATTAGTG+TATGTAGT/2 147 NC_088854.1_CT_converted 32160648 18 114M = 32160553 -209 GTTGAATTATGTTGAAGTTTTTTATTTTGTAAAATGATATAAGATGAATTTTGATTTTTTTATAGGTGAATAATAATTTTATATGATTGATTTAATATTAAAGGTGATTTTTAG FFFFF:FFFFFFFF,FFFFFFF,FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF:FFFFFFFFFFFFFFFFFFFFFF (ERR): bowtie2-align died with signal 13 (PIPE) (ERR): bowtie2-align died with signal 13 (PIPE) Work dir: /mmfs1/gscratch/scrubbed/strigg/analyses/20250401_methylseq/work/39/114b73bfc07d4bb5a7efa62b9e82f6 Container: /gscratch/scrubbed/srlab/.apptainer/depot.galaxyproject.org-singularity-bismark-0.24.2--hdfd78af_0.img Tip: you can try to figure out what's wrong by changing to the process work dir and showing the script file named `.command.sh`
nextflow run nf-core/methylseq -c /gscratch/srlab/strigg/bin/uw_hyak_srlab.config --input /gscratch/scrubbed/strigg/analyses/20250401_methylseq/samplesheet.csv --outdir /gscratch/scrubbed/strigg/analyses/20250401_methylseq --fasta /gscratch/srlab/sr320/github/project-oyster-oa/data/Haws-11/GCF_963853765.1_xbMagGiga1.1_genomic.fa -resume -with-report nf_report.html -with-trace -with-timeline nf_timeline.html --skip_trimming --nomeseq
78f1f08d9049bd123f3defd84fae2dbc
87cdc1b4-b87b-4964-88f6-9044c3539982
https://github.com/nf-core/methylseq
, revision master
(commit hash d16f8f81e812d86f4d297e69de3f001628dfd5b4
)These plots give an overview of the distribution of resource usage for each process.
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