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We classified an HCDiff as heteroplasmic if: (1) the variant frequency was between 0.10 and 0.80 and (2) all non-variant reads contained only the reference allele, and as homoplasmic if: (1) variant frequency was ≥0.80 and (2) all non-variant reads may be explained by a homopolymer error that occurred at or adjacent to the nucleotide position.
The overall MUTYH variant frequency was 0.34%.
Minimum variant frequency was set to zero, to allow comparison with ShoRAH.
The SNP variant frequency was plotted against the SNP chromosomal position.
In the case of mosaicism experiments, variant frequency was also evaluated.
The SNP variant frequency was subsequently plotted against the respective chromosomal position of the SNP.
Similar(41)
On the basis of these differences, filters on variant frequency were chosen to select for reproducible calls.
When the variant frequency is larger than 1% in a population, it is called a copy number polymorphism (CNP).
Likewise, no differences in MT- ND1 T4216C variant frequency were observed.
Changing the ratio affects the probability with which an observed relative variant frequency is interpreted by the model as a phenotype linked region (see also below).
Variant frequency is shown to fluctuate mostly in the capsid gene region as positive selection persists to enable cell-tropism subsequent to propagation system changes.
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