Barely Significant
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Genome-wide survey of allele-specific splicing in humans.

BMC Genomics · 2008 · PMC2427040 · PMID 18518984

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highly significantno p-value reported
This association can be highly significant if there are many ESTs of the gene in the two cDNA libraries in which it occurs.

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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.