Entering edit mode
4.0 years ago
Pac314
▴
10
I have 2 samples with 3 replicates each having PE reads. If I run:
STAR --genomeDir genomeDir/ \
--readFilesIn Sample1-rep1-read1,sample1-rep2-read1,sample1-rep3-read1, sample1-rep1-read2,sample1-rep2-read2,sample1-rep3-read2
--runThreadN 8 \
--outSAMtype BAM SortedByCoordinate \
--quantMode GeneCounts
STAR --genomeDir genomeDir/ \
--readFilesIn Sample2-rep1-read1,sample2-rep2-read1,sample2-rep3-read1, Sample2-rep1-read2,sample2-rep2-read2,sample2-rep3-read2\
--runThreadN 8 \
--outSAMtype BAM SortedByCoordinate \
--quantMode GeneCounts
I get only this ouput in my ReadsPerGene.out.tab:
N_unmapped 1101143 1101143 1101143
N_multimapping 118148 118148 118148
N_noFeature 780486 2709783 2726521
N_ambiguous 0 0 0
Should I run a single star command on each read pair using a loop instead?
Yea, if you don't provide the argument
--outFileNamePrefix
it will name everything the same (and thus overwrite previous files).Ah silly me! Thank you!