Article

The unreachable genomic profiling of complex diseases: genotype missingness matters

2025-07-31

Abstract excerpt

The problem of building genome-wide predictors of individual risk to complex diseases seems to be more challenging than it was thought when the first human genome was sequenced on 2003. We have build different enhanced genetic risk predictors from genome-wide data and different complex diseases, making use of haplotypes accurately ascertained from family trios. We confirmed the widely known inability to accurately...

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Literature Corpus work: ce61c5f4-3482-515c-abd3-59a8e115b5f1
DOI: 10.1101/2025.07.27.667026

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