Will the future of knowledge work automation transform personalized medicine?

Appl Transl Genom · 2014 · PMC4886728 · PMID 27284504

Europe PMC DOI

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highly significantno p-value reported

Further, clinical researchers and geneticist will be equipped with highly significant genotype–phenotype data, to use towards developing new assays, chips and tests for novel disease causing variants for prenatal diagnostics.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.