Hi STAR community! I am trying to run the following script:
STAR-2.5.2a/source/STAR --runThreadN 24 --genomeDir mus_OrthoSet4_STARIndex --readFilesIn M3FL1_S1_L004_R1_001_Trimmed.fastq --outSAMtype BAM SortedByCoordinate --quantMode TranscriptomeSAM GeneCounts --sjdbGTFfile mus_OrthoSet4_STARIndex/musAnno4_1To1Orthologs.gtf --outFileNamePrefix M3F1_OrthoSet4
The .out for this job reports 'finished successfully'. I can see 89.48% reads mapped uniquely to the reference in the Log.final.out.
However, I get an error that reports --outSAMtype: command not found. I also do not see any of the following expected outputs-
ReadsPerGene.out.tab
sortedByCoord.out.bam
toTranscriptome.out.bam
STARgenome (directory)
Shall be very grateful for any advice or help!!