Barely Significant
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Genome Medicine: past, present and future.

Genome Med · 2011 · PMC3092091 · PMID 21345269

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highly significantno p-value reported
Whether or not WES or WGS will discern repeat expansion, a highly significant form of pathology-associated genetic variation, also remains to be demonstrated.

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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.