<i>De novo</i> diploid genome assembly for genome-wide structural variant detection.

NAR Genom Bioinform · 2020 · PMC7671403 · PMID 33575568

Europe PMC DOI

hedged sentence

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closest p · 0.0× alpha

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boldest claim

The sentences

highly significantP < 10E-24actually significant

This represents a highly significant (Chi-square test, P < 10E-24) deviation from expectation (108 deletions, 106 insertions, based on their proportion in the set of 5167 SVs that could be aligned to both apes).

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