Barely Significant
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CRISPR/Cas9 screening using unique molecular identifiers.

Mol Syst Biol · 2017 · PMC5658704 · PMID 28993443

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highly significantno p-value reported
The number of highly significant hit genes (as defined by a false discovery rate smaller than 1%) was massively increased in IRA/SSMD and lineage dropout analysis when compared to total read count analysis (Fig 3 C).

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