Hello guys I'm working on Rna SEQ data, and I want to get good conceptual knowledge about the analysis of the process.
I used the tool bowtie for indexing my reference genome and then the rest is according to the TUXEDO pipeline.
I don't understand what exactly, "indexing" of the reference genome is and why it had to be done.
I do get the point that there are many genes that can be identified and can be matched to the genome and indexed, But i am not clear as ti why should we do this , how is it done . ( i am new to bioinformatics and with minimal knowledge its so hard to understand the algorithm part of it )
so can anyone put it in simple concepts .