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Mapping reads to a very small reference

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!

bowtie2 mapping

2 answers

You could but if you have data that came from entire genome/larger reference then you can get some spurious mapping (reads mapping even though they may not have originated from the ~2.7K bases). It would be best to map to entire genome and then extract reads that span regions of interest.

You can do it but is much better to map to genome of interest and then extract the region you are interested in

duplicated reply sorry! I haven't seen the other reply when I was writing

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