Thanks Devon for your quick reply. The % alignment rate was very low (~2-20%) when the sample reads were mapped against the individual genome fasta file, however, the alignment % significantly increased (~60-80%) when the sample reads were mapped against the transcriptome alone. I am unsure which one to use for downstream differential expression analysis using Stringtie etc. ps: I did not use the gff for building index, only used either the genome or transcriptome fasta file for creating index.
Any suggestions please? Many thanks