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Chunk #27 — Experimental design — Setting tag family size by PCR amplification

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Detecting ultralow-frequency mutations by Duplex Sequencing.
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to raise the number of raw reads needed to form a single DCS to ~40. Notably, this formula provides a rough estimate of the depth that will be obtained provided that the peak family size and SSCS:DCS ratio are optimal. After determining the per-sample lane fraction, this value can be referred to in Table 2 to determine the amount of target DNA that should be used in the PCR to obtain the appropriate peak family size of six.