Hi, I am trying to get the kmers that are uniquely located within my region of interest on the genome. I got with KMC lists of kmers in my range (I tried different lengths) and now I would like to use this multi-fasta list to align them in GRCH38 and see if they map only there or also elsewhere. I am trying to do the alignment with Bowtie because it works better with short alignments (I have kmers of max 35 bp). Once I get my .sam file with the alignment how can I identify which kmers in my list map only in my range and which map elsewhere and where?
Thank you I'll take a look!