Barely Significant
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ABSSeq: a new RNA-Seq analysis method based on modelling absolute expression differences.

BMC Genomics · 2016 · PMC4973090 · PMID 27488180

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highly significantno p-value reported
These tests neglect the magnitude of encountered differences and might report statistically highly significant DE with arbitrarily small fold change, at least if the number of sequencing counts is large enough [ 6 , 7 ].

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