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This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

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Abstract

Figure S1. The analytical sensitivity and specificity of the CADMA assays performed using the Rotorgene Q. Ten wild-type replicates were run together with a standard dilution series of mutant alleles from cell lines carrying the relevant mutations in a wild-type background (50%, 10%, 1%, and 0.5%) in triplicates. The three replicates of the 0.5% standard could all be distinguished from ten wild-type replicates in all assays. A. The c.34 G > A CADMA assay. B. The c.38 G > A CADMA assay. C. The c.35 G > A CADMA assay. D. The c.34 G > C CADMA assay. E. The c.35 G > T CADMA assay. F. The c.34 G > T CADMA assay.