Barely Significant
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Genetic background drives transcriptional variation in human induced pluripotent stem cells.

PLoS Genet · 2014 · PMC4046971 · PMID 24901476

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highly significantno p-value reported
Likewise, for individuals in our dataset that are heterozygous at the eSNP we see a corresponding, highly significant allelic imbalance also in the expected direction ( Fig. 4c ).

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