| 摘要 |
Homogenous detection during or following PCR amplification, preferably LATE-PCR, utilizing fluorescent DNA dye and indirectly excitable labelled primers and probes improves reproducibility and quantification. Low-temperature homogenous detection during or following non-symmetric PCR amplification, preferably LATE-PCR, utlilizing fluorescent DNA dye and indirectly excitable labeled mismatch-tolerant probes permits analysis of complex targets. Sequencing sample preparation methods following LATE-PCR amplifications reduce complexity and permit "single-tube" processing. |
