i force installed the 2.6.1d so now it works. Also i downloaded the plug and play genome resource library so i guess thats ok. My command is :
STAR-Fusion --left_fq GlentisS1_S17_R1_001.fastq.gz --right_fq GlentisS1_S17_R2_001.fastq.gz --genome_lib_dir '/..../GRCh38_v27_CTAT_lib_Feb092018/ctat_genome_lib_build_dir' --CPU 10 --output_dir STAR-Fusion_outdir/
But the outcome is :
CMD: mkdir -p /home/app/Desktop/Untitled Folder/GlentisRNASeq/top_dir/STAR-Fusion_outdir//_starF_checkpoints
CMD: mkdir -p /home/app/Desktop/Untitled Folder/GlentisRNASeq/top_dir/STAR-Fusion_outdir//star-fusion.preliminary
* Running CMD: /home/app/anaconda3/bin/STAR --genomeDir /media/app/New_Volume/jim/reference/Star-Fusion_genome_resource_lib/hg38/GRCh38_v27_CTAT_lib_Feb092018/ctat_genome_lib_build_dir/ref_genome.fa.star.idx --outReadsUnmapped None --chimSegmentMin 12 --chimJunctionOverhangMin 12 --chimOutJunctionFormat 1 --alignSJDBoverhangMin 10 --alignMatesGapMax 100000 --alignIntronMax 100000 --alignSJstitchMismatchNmax 5 -1 5 5 --runThreadN 10 --outSAMstrandField intronMotif --outSAMunmapped Within --outSAMtype BAM Unsorted --readFilesIn /home/app/Desktop/Untitled Folder/GlentisRNASeq/top_dir/GlentisS1_S17_R1_001.fastq.gz /home/app/Desktop/Untitled Folder/GlentisRNASeq/top_dir/GlentisS1_S17_R2_001.fastq.gz --outSAMattrRGline ID:GRPundef --chimMultimapScoreRange 10 --chimMultimapNmax 10 --chimNonchimScoreDropMin 10 --peOverlapNbasesMin 12 --peOverlapMMp 0.1 --genomeLoad NoSharedMemory --twopassMode Basic --readFilesCommand 'gunzip -c'
gzip: /home/app/Desktop/Untitled is a directory -- ignored
gzip: Folder/GlentisRNASeq/top_dir/GlentisS1_S17_R1_001.fastq.gz: No such file or directory
gzip: /home/app/Desktop/Untitled is a directory -- ignored
Segmentation fault (core dumped)
Error, cmd: /home/app/anaconda3/bin/STAR --genomeDir /media/app/New_Volume/jim/reference/Star-Fusion_genome_resource_lib/hg38/GRCh38_v27_CTAT_lib_Feb092018/ctat_genome_lib_build_dir/ref_genome.fa.star.idx --outReadsUnmapped None --chimSegmentMin 12 --chimJunctionOverhangMin 12 --chimOutJunctionFormat 1 --alignSJDBoverhangMin 10 --alignMatesGapMax 100000 --alignIntronMax 100000 --alignSJstitchMismatchNmax 5 -1 5 5 --runThreadN 10 --outSAMstrandField intronMotif --outSAMunmapped Within --outSAMtype BAM Unsorted --readFilesIn /home/app/Desktop/Untitled Folder/GlentisRNASeq/top_dir/GlentisS1_S17_R1_001.fastq.gz /home/app/Desktop/Untitled Folder/GlentisRNASeq/top_dir/GlentisS1_S17_R2_001.fastq.gz --outSAMattrRGline ID:GRPundef --chimMultimapScoreRange 10 --chimMultimapNmax 10 --chimNonchimScoreDropMin 10 --peOverlapNbasesMin 12 --peOverlapMMp 0.1 --genomeLoad NoSharedMemory --twopassMode Basic --readFilesCommand 'gunzip -c' died with ret 35584 No such file or directory at /home/app/anaconda3/lib/STAR-Fusion/PerlLib/Pipeliner.pm line 181.
Pipeliner::run(Pipeliner=HASH(0x55ed47235e50)) called at /home/app/anaconda3/lib/STAR-Fusion/STAR-Fusion line 862
main::run_STAR(Pipeliner=HASH(0x55ed47235e50), "/home/app/Desktop/Untitled Folder/GlentisRNASeq/top_dir/Glent"..., "/home/app/Desktop/Untitled Folder/GlentisRNASeq/top_dir/Glent"..., "") called at /home/app/anaconda3/lib/STAR-Fusion/STAR-Fusion line 509
When i try with .fastq rather than .fastq.gz i get fatal error
ERROR EXITING because of fatal input ERROR: could not open readFilesIn=Folder/GlentisRNASeq/top_dir/GlentisS1_S17_R1_001.fastq
According to this Tweet rather use
conda create -n star-fusion -c bioconda star-fusionand activate the environment each time you want to run star-fusion.thanks a lot. I installed it like you said. But when i type :
nothing happens. I also tried after activating enviroment :
but still nothing