Barely Significant
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A chromatin code for alternative splicing involving a putative association between CTCF and HP1α proteins.

BMC Biol · 2015 · PMC4446157 · PMID 25934638

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likely to be significantno p-value reported
As the coverage of reads between samples and control can be highly variable, in order to estimate the background level, we considered that each sample is composed of a number of regions with high coverage, likely to be significant, and a large number of regions with low coverage, assumed to be equivalent to the background [ 68 , 69 ].

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