======================================== nf-core/eager v2.0.2 ======================================== Run Name: naughty_lorenz #################################################### ## nf-core/eager 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 > 'bwa (ABM006.A0101_S0_L002_R1_001)' Caused by: Process `bwa (ABM006.A0101_S0_L002_R1_001)` terminated with an error exit status (1) Command executed: bwa aln -t 1 hg19_MT.fasta ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.gz -n 0.04 -l 32 -k 2 -f "ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.sai" bwa samse -r "@RG\tID:ILLUMINA-ABM006.A0101_S0_L002_R1_001\tSM:ABM006.A0101_S0_L002_R1_001\tPL:illumina" hg19_MT.fasta "ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq".sai ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.gz | samtools sort -@ 1 -O bam - > "ABM006.A0101_S0_L002_R1_001".sorted.bam samtools index -@ 1 "ABM006.A0101_S0_L002_R1_001".sorted.bam Command exit status: 1 Command output: (empty) Command error: [bwa_aln_core] calculate SA coordinate... 1.14 sec [bwa_aln_core] write to the disk... 0.01 sec [bwa_aln_core] 1835008 sequences have been processed. [bwa_aln_core] calculate SA coordinate... 0.93 sec [bwa_aln_core] write to the disk... 0.01 sec [bwa_aln_core] 2027689 sequences have been processed. [main] Version: 0.7.12-r1039 [main] CMD: bwa aln -t 1 -n 0.04 -l 32 -k 2 -f ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.sai hg19_MT.fasta ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.gz [main] Real time: 13.003 sec; CPU: 12.988 sec [bwa_aln_core] convert to sequence coordinate... 0.02 sec [bwa_aln_core] refine gapped alignments... 0.02 sec [bwa_aln_core] print alignments... 0.21 sec [bwa_aln_core] 262144 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.04 sec [bwa_aln_core] refine gapped alignments... 0.05 sec [bwa_aln_core] print alignments... 0.21 sec [bwa_aln_core] 524288 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.06 sec [bwa_aln_core] refine gapped alignments... 0.04 sec [bwa_aln_core] print alignments... 0.19 sec [bwa_aln_core] 786432 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.02 sec [bwa_aln_core] refine gapped alignments... 0.02 sec [bwa_aln_core] print alignments... 0.19 sec [bwa_aln_core] 1048576 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.02 sec [bwa_aln_core] refine gapped alignments... 0.02 sec [bwa_aln_core] print alignments... 0.19 sec [bwa_aln_core] 1310720 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.02 sec [bwa_aln_core] refine gapped alignments... 0.02 sec [bwa_aln_core] print alignments... 0.19 sec [bwa_aln_core] 1572864 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.03 sec [bwa_aln_core] refine gapped alignments... 0.05 sec [bwa_aln_core] print alignments... 0.21 sec [bwa_aln_core] 1835008 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.02 sec [bwa_aln_core] refine gapped alignments... 0.04 sec [bwa_aln_core] print alignments... 0.15 sec [bwa_aln_core] 2027689 sequences have been processed. [main] Version: 0.7.12-r1039 [main] CMD: bwa samse -r @RG\tID:ILLUMINA-ABM006.A0101_S0_L002_R1_001\tSM:ABM006.A0101_S0_L002_R1_001\tPL:illumina hg19_MT.fasta ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.sai ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.gz [main] Real time: 7.227 sec; CPU: 6.184 sec index: invalid option -- '@' Usage: samtools index [-bc] [-m INT] [out.index] Options: -b Generate BAI-format index for BAM files [default] -c Generate CSI-format index for BAM files -m INT Set minimum interval size for CSI indices to 2^INT [14] Work dir: /projects1/users/fellows/nextflow/eager2/my_test/work/09/867e241abeeb78307c9fc618980ca2 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` #################################################### ## nf-core/eager 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 > 'bwa (ABM006.A0101_S0_L002_R1_001)' Caused by: Process `bwa (ABM006.A0101_S0_L002_R1_001)` terminated with an error exit status (1) Command executed: bwa aln -t 1 hg19_MT.fasta ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.gz -n 0.04 -l 32 -k 2 -f "ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.sai" bwa samse -r "@RG\tID:ILLUMINA-ABM006.A0101_S0_L002_R1_001\tSM:ABM006.A0101_S0_L002_R1_001\tPL:illumina" hg19_MT.fasta "ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq".sai ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.gz | samtools sort -@ 1 -O bam - > "ABM006.A0101_S0_L002_R1_001".sorted.bam samtools index -@ 1 "ABM006.A0101_S0_L002_R1_001".sorted.bam Command exit status: 1 Command output: (empty) Command error: [bwa_aln_core] calculate SA coordinate... 1.14 sec [bwa_aln_core] write to the disk... 0.01 sec [bwa_aln_core] 1835008 sequences have been processed. [bwa_aln_core] calculate SA coordinate... 0.93 sec [bwa_aln_core] write to the disk... 0.01 sec [bwa_aln_core] 2027689 sequences have been processed. [main] Version: 0.7.12-r1039 [main] CMD: bwa aln -t 1 -n 0.04 -l 32 -k 2 -f ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.sai hg19_MT.fasta ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.gz [main] Real time: 13.003 sec; CPU: 12.988 sec [bwa_aln_core] convert to sequence coordinate... 0.02 sec [bwa_aln_core] refine gapped alignments... 0.02 sec [bwa_aln_core] print alignments... 0.21 sec [bwa_aln_core] 262144 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.04 sec [bwa_aln_core] refine gapped alignments... 0.05 sec [bwa_aln_core] print alignments... 0.21 sec [bwa_aln_core] 524288 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.06 sec [bwa_aln_core] refine gapped alignments... 0.04 sec [bwa_aln_core] print alignments... 0.19 sec [bwa_aln_core] 786432 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.02 sec [bwa_aln_core] refine gapped alignments... 0.02 sec [bwa_aln_core] print alignments... 0.19 sec [bwa_aln_core] 1048576 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.02 sec [bwa_aln_core] refine gapped alignments... 0.02 sec [bwa_aln_core] print alignments... 0.19 sec [bwa_aln_core] 1310720 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.02 sec [bwa_aln_core] refine gapped alignments... 0.02 sec [bwa_aln_core] print alignments... 0.19 sec [bwa_aln_core] 1572864 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.03 sec [bwa_aln_core] refine gapped alignments... 0.05 sec [bwa_aln_core] print alignments... 0.21 sec [bwa_aln_core] 1835008 sequences have been processed. [bwa_aln_core] convert to sequence coordinate... 0.02 sec [bwa_aln_core] refine gapped alignments... 0.04 sec [bwa_aln_core] print alignments... 0.15 sec [bwa_aln_core] 2027689 sequences have been processed. [main] Version: 0.7.12-r1039 [main] CMD: bwa samse -r @RG\tID:ILLUMINA-ABM006.A0101_S0_L002_R1_001\tSM:ABM006.A0101_S0_L002_R1_001\tPL:illumina hg19_MT.fasta ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.sai ABM006.A0101_S0_L002_R1_001.combined.prefixed.fq.gz [main] Real time: 7.227 sec; CPU: 6.184 sec index: invalid option -- '@' Usage: samtools index [-bc] [-m INT] [out.index] Options: -b Generate BAI-format index for BAM files [default] -c Generate CSI-format index for BAM files -m INT Set minimum interval size for CSI indices to 2^INT [14] Work dir: /projects1/users/fellows/nextflow/eager2/my_test/work/09/867e241abeeb78307c9fc618980ca2 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` The workflow was completed at Wed Nov 14 17:08:40 CET 2018 (duration: 2m 58s) The command used to launch the workflow was as follows: nextflow run nf-core/eager --reads /projects1/users/fellows/nextflow/eager2/my_test/data/ABM006.A0101/*_R{1,2}*fastq.gz --pairedEnd --fasta /projects1/users/fellows/nextflow/eager2/my_test/references/hg19_MT.fasta --outdir /projects1/users/fellows/nextflow/eager2/my_test/output_eager2 -profile singularity --max_cpus 4 --max_memory 16G -r 2.0.2 Pipeline Configuration: ----------------------- - Pipeline Name: nf-core/eager - Pipeline Version: 2.0.2 - Run Name: naughty_lorenz - Reads: /projects1/users/fellows/nextflow/eager2/my_test/data/ABM006.A0101/*_R{1,2}*fastq.gz - Fasta Ref: /projects1/users/fellows/nextflow/eager2/my_test/references/hg19_MT.fasta - Data Type: Paired-End - Max Memory: 16G - Max CPUs: 4 - Max Time: null - Output dir: /projects1/users/fellows/nextflow/eager2/my_test/output_eager2 - Working dir: /projects1/users/fellows/nextflow/eager2/my_test/work - Container Engine: singularity - Container: [:] - Current home: /projects1/clusterhomes/fellows - Current user: fellows - Current path: /projects1/users/fellows/nextflow/eager2/my_test - Script dir: /projects1/clusterhomes/fellows/.nextflow/assets/nf-core/eager - Config Profile: singularity - Date Started: Wed Nov 14 17:05:42 CET 2018 - Date Completed: Wed Nov 14 17:08:40 CET 2018 - Pipeline script file path: /projects1/clusterhomes/fellows/.nextflow/assets/nf-core/eager/main.nf - Pipeline script hash ID: b830dc186a77957a7b56fd9b3a6233ea - Pipeline repository Git URL: https://github.com/nf-core/eager.git - Pipeline repository Git Commit: c44b88110d7daba8b51c6a0aca96be74b30d8afd - Pipeline Git branch/tag: 2.0.2 - Nextflow Version: 0.32.0 - Nextflow Build: 4897 - Nextflow Compile Timestamp: 27-09-2018 10:17 UTC -- nf-core/eager https://github.com/nf-core/eager