Barely Significant
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Novel insights into systemic sclerosis using a sensitive computational method to analyze whole-genome bisulfite sequencing data.

Clin Epigenetics · 2023 · PMC10239181 · PMID 37270501

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highly significantno p-value reported
The number of overlapping CpG sites was higher (larger points) for the subset of CpG regions that were identified as highly significant in both methods (top right quadrant of the plots).

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