Barely Significant
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A forest-based feature screening approach for large-scale genome data with complex structures.

BMC Genet · 2015 · PMC4690313 · PMID 26698561

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a clear trendno p-value reported
With such a clear trend, no one will doubt whether all SNPs other than the two peaks are type I error or truly causative genetic variants.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.