Hi has any one got any advice on a two-step PCR amplicon library generation via barcode/adapter addition using a secondary PCR.
I am using the Fluidigm AA system have generated my Primary PCR amplicons 48 samples each with 48 amplocons and now need to attach the barcode/adapter via a secondary PCR. Fluidigm suggest using a 1in100 dilution of the primary PCR and adding the adapters using 15 cycles in a 20uL PCR.
My question is would it not be better to use a less dilute amount of the primary PCR say 1in20 or 1in40 dilution and cut the number of cycles to 12 or 13 and even in half the reaction volume (say 10uL), therefore reducing PCR errors by using fewer additional cycles? I just wondered if these modifications would be beneficial?
Thanks
I am using the Fluidigm AA system have generated my Primary PCR amplicons 48 samples each with 48 amplocons and now need to attach the barcode/adapter via a secondary PCR. Fluidigm suggest using a 1in100 dilution of the primary PCR and adding the adapters using 15 cycles in a 20uL PCR.
My question is would it not be better to use a less dilute amount of the primary PCR say 1in20 or 1in40 dilution and cut the number of cycles to 12 or 13 and even in half the reaction volume (say 10uL), therefore reducing PCR errors by using fewer additional cycles? I just wondered if these modifications would be beneficial?
Thanks
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