Barely Significant
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Ultrasensitive and high-efficiency screen of de novo low-frequency mutations by o2n-seq.

Nat Commun · 2017 · PMC5458117 · PMID 28530222

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extremely significantP <0.001actually significant
Results indicated that the number of TP mutations detected by o2n-seq were extremely significant (all P <0.001, Student's t -test) more than that of Cir-seq for any CSs criteria (1 × −5 × ) ( Supplementary Fig. 4a ).

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