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The implementation of genome sequencing in rare genetic diseases diagnosis: a pilot study from the Hong Kong genome project.

Lancet Reg Health West Pac · 2025 · PMC11814671 · PMID 39944418

Europe PMCDOI
1
hedged sentence
0.6020
closest p · 12.0× alpha
0.6020
boldest claim

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showed a trendp = 0.602not close (p > 0.1)
No significant difference in diagnostic yield was found among different family structures while cases that were sequenced as larger family structure showed a trend to be higher than those that were sequenced as singletons (33.7% vs 25.7; p = 0.602) ( Fig. 2 a).

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