Barely Significant
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A robust estimation of exon expression to identify alternative spliced genes applied to human tissues and cancer samples.

BMC Genomics · 2014 · PMC4298068 · PMID 25297679

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highly significantno p-value reported
Furthermore, we performed a validation analysis on human patient samples comparing two different subtypes of acute myeloid leukemia (AML) and we experimentally validated the splicing in several selected genes that showed exons with highly significant signal change.

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