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Chunk #55 — Materials and methods — Mutation detection procedure — Step 2b: determination of the statistical significance

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Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing.
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Given the estimated error rate E, the read depth N and the count of alternative allele X, a binomial model was used to compute the P-value for the event that more than X alternative alleles were observed when the null hypothesis is true. When a position is covered by both forward and reverse reads, we used the Stouffer's Z-score method (weighted by the read depths) to combine P-values of individual tests into a single P-value.