Hi friends, I am learning RNA_Seq. I want to know the actual function of bowtie. For my understanding bowtie takes reference genome file (.fa) as an input after that it generates .bt2 files as an output. In my point of view this step for indexing (string compression for aligning). Bowtie also used for aligning at this point I was confused. In what step bowtie do align and what are the input files. please explain. I know this is a simple question. But I got stuck.
Please don't tag your question as "software error" if there is no software error. I have corrected your tags.