02 December 2020 2 9K Report

Hi!

We are targeting a gene that has ~100 genotype. We want to design a multiplex primers to capture it from cDNA and doing sequencing afterwards

Thus non-specific or degenerate primers are fine for this purpose. However the primers cannot have self-dimer, cross-dimer and dimer with PE1, PE2 (Adaptor for P5, P7 Illumina dye sequencing), how should we set the FastPCR parameters?

Thanks!

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