Hi Alex,
Is it possible to run STAR for mapping, remove duplicates reads and read counts in a single command ? (I have 3' RNAseq data)
Like this:
STAR --runThreadN 16 --genomeDir STAR_GTF --readFilesIn Read1.fastq --readFilesCommand zcat --outFileNamePrefix $name --outSAMtype \
BAM SortedByCoordinate --limitBAMsortRAM 50000000000 --chimSegmentMin 20 -- --bamRemoveDuplicatesType UniqueIdentical quantMode TranscriptomeSAM GeneCounts --outReadsUnmapped Fastx --outWigType bedGraph --outWigNorm RPM
Thanks,
regards,
jacs