Successful identification of rare variants using oligogenic segregation analysis as a prioritizing tool for whole-exome sequencing studies.

BMC Proc · 2011 · PMC3287833 · PMID 22373114

Europe PMC DOI

hedged sentence

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closest p · 0.0× alpha

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boldest claim

The sentences

highly significantp = 7.9 × 10 –12actually significant

For trait Q1, C4S4935 ( VEGFC ) explained a highly significant proportion of the variance (33.1% in family 7, p = 7.9 × 10 –12 ; 10.6% in all families combined, p = 1.1 × 10 –16 ).

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