Barely Significant
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A spectral approach integrating functional genomic annotations for coding and noncoding variants.

Nat Genet · 2016 · PMC4731313 · PMID 26727659

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highly significantno p-value reported
Overall results are highly significant for all the different methods, with the Eigen score performing better than the Eigen-PC and the CADD-score in most of the cases.

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