if [ -f RAP1_IAA_30M_REP1.Unmapped.out.mate1 ]; then
mv RAP1_IAA_30M_REP1.Unmapped.out.mate1 RAP1_IAA_30M_REP1.unmapped_1.fastq
gzip RAP1_IAA_30M_REP1.unmapped_1.fastq
fi
if [ -f RAP1_IAA_30M_REP1.Unmapped.out.mate2 ]; then
mv RAP1_IAA_30M_REP1.Unmapped.out.mate2 RAP1_IAA_30M_REP1.unmapped_2.fastq
gzip RAP1_IAA_30M_REP1.unmapped_2.fastq
fi
Version: 24.10.0 build 5928
Created: 27-10-2024 18:36 UTC (14:36 EDT)
System: Mac OS X 15.1
Runtime: Groovy 4.0.23 on OpenJDK 64-Bit Server VM 11.0.13+7-b1751.21
Encoding: UTF-8 (UTF-8)
Description of the bug
STAR command fails to produce output in linux/amd64 mode on macOS arm64/v8 in docker profile
Command used and terminal output
% nextflow run nf-core/rnaseq -profile rnaseq,docker -process.containerOptions "--platform linux/amd64"
...
Execution cancelled -- Finishing pending tasks before exit -[nf-core/rnaseq] Pipeline completed with errors- ERROR ~ Error executing process > 'NFCORE_RNASEQ:RNASEQ:ALIGN_STAR:STAR_ALIGN (RAP1_IAA_30M_REP1)'
Caused by: Missing output file(s)
*Log.final.out
expected by processNFCORE_RNASEQ:RNASEQ:ALIGN_STAR:STAR_ALIGN (RAP1_IAA_30M_REP1)
Command executed:
STAR \ --genomeDir star \ --readFilesIn input1/RAP1_IAA_30M_REP1_primary_1.fastq.gz input2/RAP1_IAA_30M_REP1_primary_2.fastq.gz \ --runThreadN 4 \ --outFileNamePrefix RAP1_IAA_30M_REP1. \ \ --sjdbGTFfile genome_gfp.gtf \ --outSAMattrRGline 'ID:RAP1_IAA_30M_REP1' 'SM:RAP1_IAA_30M_REP1' \ --quantMode TranscriptomeSAM --twopassMode Basic --outSAMtype BAM Unsorted --readFilesCommand zcat --runRNGseed 0 --outFilterMultimapNmax 20 --alignSJDBoverhangMin 1 --outSAMattributes NH HI AS NM MD --outSAMstrandField intronMotif --quantTranscriptomeSAMoutput BanSingleEnd
if [ -f RAP1_IAA_30M_REP1.Unmapped.out.mate1 ]; then mv RAP1_IAA_30M_REP1.Unmapped.out.mate1 RAP1_IAA_30M_REP1.unmapped_1.fastq gzip RAP1_IAA_30M_REP1.unmapped_1.fastq fi if [ -f RAP1_IAA_30M_REP1.Unmapped.out.mate2 ]; then mv RAP1_IAA_30M_REP1.Unmapped.out.mate2 RAP1_IAA_30M_REP1.unmapped_2.fastq gzip RAP1_IAA_30M_REP1.unmapped_2.fastq fi
cat <<-END_VERSIONS > versions.yml "NFCORE_RNASEQ:RNASEQ:ALIGN_STAR:STARALIGN": 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_VERSIONS
Command exit status: 0
Command output: (empty)
Work dir: /Users/pikalaxalt/nextflow-launch-directories/work/d2/c757228cbe86dafe7412bc3d1afd2d
Container: quay.io/nf-core/star_samtools_htslib_gawk:10c6e8c834460019
Tip: when you have fixed the problem you can continue the execution adding the option
-resume
to the run command line-- Check '.nextflow.log' file for details ERROR ~ Pipeline failed. Please refer to troubleshooting docs: https://nf-co.re/docs/usage/troubleshooting
-- Check '.nextflow.log' file for details
Relevant files
Version: 24.10.0 build 5928 Created: 27-10-2024 18:36 UTC (14:36 EDT) System: Mac OS X 15.1 Runtime: Groovy 4.0.23 on OpenJDK 64-Bit Server VM 11.0.13+7-b1751.21 Encoding: UTF-8 (UTF-8)
Core Nextflow options revision : master runName : serene_bhabha containerEngine : docker launchDir : /Users/pikalaxalt/nextflow-launch-directories workDir : /Users/pikalaxalt/nextflow-launch-directories/work projectDir : /Users/pikalaxalt/.nextflow/assets/nf-core/rnaseq userName : pikalaxalt profile : docker,test configFiles :
nextflow version: 24.10.0 hardware: macbook executor: local container engine: docker os: macos 15.1 silicon (arm64 v8) version of nf-core/rnaseq: 00f924cf92a986a842bb352b3c4ae379c773c989
System information
No response