I' try to detect the differentially expressed gene using human RNASEQ data. And I don't care about the  alternative splice and so on right now.

Could I just use tophat to map my reads and cuffdiff to deal with the bam file and get the DEG?

Or I must follow the tophat-cufflink-coffmerge-cuffdiff pipeline strictly?

I have got the gtf file from UCSC and iGenome.

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