I was using a public RNA-Seq dataset and was exploring the insights and saw that the miRNA had very low counts compared to the other RNAs and it is logical, I was using STAR with gencode fasta file and gtf files
So, I was trying to use bowtie and miRdeep for alignment using miRbase fasta and gtf files to enrich and focus on the miRNAs in my dataset and I keep getting zero alignments and I am using the default settings wanting to retrieve only the miRNA sequences
Thanks for explaining the situation. From a first guess, the issue is either the reference data, or the alignment parameters, or the mapping tool choice.
We have an example in this tutorial – maybe it helps to frame the analysis space?