Barely Significant
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Prioritizing single-nucleotide polymorphisms and variants associated with clinical mastitis.

Adv Appl Bioinform Chem · 2017 · PMC5473491 · PMID 28652783

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highly significantno p-value reported
27 A blast search with the well-reported human lncRNAs from databases such as Noncode ( www.noncode.org ) and the highly significant regions that meet the e-value (expectant value) threshold of <0 are considered.

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