The phrase "average variant" is correct and usable in written English.
It can be used in contexts where you are discussing a typical or common version of something, often in comparison to other variants.
Example: "In our study, we found that the average variant of the product performed better than the others in terms of customer satisfaction."
Alternatives: "typical version" or "standard variant".
The Granger Ramanathan average variant C (GRC) is recommended as the best compromise between accuracy, speed of execution, and simplicity.
The resulting 12 hydrographs (4 models × 3 metrics) were weighted and combined with the help of 9 averaging methods which are the simple arithmetic mean (SAM), Akaike information criterion (AICA), Bates Granger (BGA), Bayes information criterion (BICA), Bayesian model averaging (BMA), Granger Ramanathan average variant A, B and C (GRA, GRB and GRC) and the average by SCE-UA optimization (SCA).
A total of 3,036,468 variants (2,765,215 SNPs and 292,003 InDels) were identified with average variant rate ranging from 91 bp on chromosome 10 to 163 bp on chromosome 2 (Additional file 1: Table S2).
For example, sites 9237 and 4458 both attained a stable variant count by 1996, however the first had an average variant count of 0.6 and the latter of 0.85 (Table 2; Figure 3).
Secondly, the average variant frequency observed for the degradation products of EBERs detected from the same sequencing run is less than 1% across the entire 34-nt read length.
The average variant density and percent heterozygous were calculated for the consensus exome INDEL set and compared against the exome SNPs and non-coding INDELs of the 1000G phase 1 integrated call set.
Variant density was calculated by dividing the average variants per individual by the size of the analyzed exome target region or non-coding genome as indicated.
Because the lengths of breakpoint intervals are also measures of local sequence identity, we tested whether they were distinct from the genome-average variant spacing.
Our sample of simulated sequence data contained 669, 219 total variants, with 436, 564 having a minor allele frequency (MAF) > 1%, and on average one variant per 179 bp.
Variant counts were summed across the whole site and the total divided by the length of the site to produce an average nucleotide variant count (N score).
Average nucleotide variant counts (N scores) were calculated for each of the 17 primer sites for each year after 1988 using the data from the genome dataset.
