Improving polygenic prediction from whole-genome sequencing data by leveraging predicted epigenomic features.

Proc Natl Acad Sci U S A · 2025 · PMC12184400 · PMID 40504151

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highly significantno p-value reported

We regard the presence of SNPs with highly significant P -values for association with the disease as an indication that the corresponding LD block contains genetic variations useful for risk modeling.

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