A cautionary tale of low-pass sequencing and imputation with respect to haplotype accuracy.

Genet Sel Evol · 2024 · PMC10785484 · PMID 38216889

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highly significantp < 0.001actually significant

The result indicated a highly significant (p < 0.001) difference in sequencing depth relative to the chromosome average for regions with eight or more haplotypes [see Additional file 1 : Table S8 and Additional file 12 : Figure S11d].

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