After running qPCR plates, we would like to analyse them using the LinRegPCR software, that allows for efficiency calculation within each well. It requires fluorescence ratio before baseline correction for background fluorescence.

However, in the 7500 SDS software, we only found 'Export'>'delta Rn' to get the baseline corrected ratio. Such baseline correction is applied during analysis and can either be automatic or manual but can not be eliminated altogether.

Has anybody ever encountered (and hopefully solved) the same difficulty?

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