Hi every one,
I don't know why I could not run the following command to align my seqencing data to the reference genome.
bowtie2 -p 8 -f -x hg19 -u ~/my_rnaseq_dat/untreated1.fa -S untreated.sam.
on the contrary, I can run the following command. put the option of -f before the input file instead of -u option.
bowtie2 -p 8 -x hg19 -f ~/my_rnaseq_dat/untreated1.fa -S untreated.sam.
Thanks a lot!
Richard
I don't know why I could not run the following command to align my seqencing data to the reference genome.
bowtie2 -p 8 -f -x hg19 -u ~/my_rnaseq_dat/untreated1.fa -S untreated.sam.
on the contrary, I can run the following command. put the option of -f before the input file instead of -u option.
bowtie2 -p 8 -x hg19 -f ~/my_rnaseq_dat/untreated1.fa -S untreated.sam.
Thanks a lot!
Richard
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