Hello there, I am using RNA seq fro cotton data and generated paired end reads of 150bp in length. I need help regarding which type of mapping will be best for dealing RNA seq data.. Should I opt for Gapped or ungapped one.. To my knowledge gapped mapping is recommended while dealing with genomic data and for transcriptomic data mapping ungapped is used.
I might be wrong so need help..
Also suggest some mapping software's for reads 150bp in length. I tried to use tophat but its not quite good.
Regards
Fizzah
ok got your point. Thank your for your help