What are the recommended tools to do gene prediction from mapped Illumina RNAseq data evidence? By gene prediction I mean the evidence-based definition of the transcripts for every coding and non-coding gene in the genome using mapped RNAseq reads. Also, can I use cufflinks if I have aligned the reads with BWA?
What do you mean by "gene prediction"? Are you trying to de novo assemble a transcriptome from RNA-seq data?