Barely Significant
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A nucleosomal approach to inferring causal relationships of histone modifications.

BMC Genomics · 2014 · PMC4046832 · PMID 24564627

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highly significantno p-value reported
By which, dominance score of each modification X is calculated by dScore ( X ) = Σ C 0 ( X , Y ) k , where C 0 ( X , Y ) denotes the significance score of X being an ancestor of Y , k is the constant to reward highly significant features.

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