Hello!
I have two short genomic sequences, ~2700 bases each. I want to map short reads (Illumina TruSeq paired-end reads) to each of the ~2700 base sequences (and not to the whole reference genome) and extract only the mapped reads. Can I do this with bowtie2, using the ~2700 base sequences as a reference? If so, do you have any advice how to change the default settings so that I can map appropriately?
Thank you so much in advance!
Thank you so much!