Barely Significant
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Parallel computation of genome-scale RNA secondary structure to detect structural constraints on human genome.

BMC Bioinformatics · 2016 · PMC4858847 · PMID 27153986

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highly significantno p-value reported
In particular, we observed a highly significant preference for base pairing over entire intronic regions as compared to their antisense sequences, as well as to intergenic regions.

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