i wondered how others who have used commercial genomics cores for RNAseq then go about performing further bioinformatics analysis (beyond the basic sequencing QC and mapping provided)?

More detail - I have 2 quotes, one from university genomics core and one from commercial genomics core to perform RNAseq on 12 samples (this is actually only 4 samples in triplicate - comparisons to be made between WT and KO human cells). There is a £5000 difference in price which is related largely to the read depth 30M vs 25M and also to the bioinformatics analysis (an extra £2500) offered by the university genomics core. They will not perform any analysis on projects not sequenced by them however.

Having never done any RNAseq before, can someone advise me on how or where I could look to help analyse the data if I went with cheaper commercial quote?

Many thanks in advance

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