Sentence examples for variants were calculated from inspiring English sources

The relative percentages of the two variants were calculated by the accompanying software and were used for the gene copy number determination.

The primers used for real time PCR analysis are depicted in Table 2. Gene expression values for the various NRXN1/2/3α and splice variants were calculated based on the comparative threshold cycle (Ct) method [47].

Relative abundances of AID splice variants were calculated by comparing dCt values.

Subsequently, the normalised transcript abundances for UPFs and CD epitopes and their variants were calculated.

Functional effects of OATP2B1 missense variants were calculated using four different algorithms (Additional file 1).

Significances for the differences between wild-type and variants were calculated by one-way ANOVA and a Dunnett's post test.

Though the minimal estimated frequency of homozygotes (or compound heterozygotes) for SLC25A13 pathogenic variants is calculated to be 1 in 20,000, the incidence of CTLN2 is much lower, at 1 in 100,000 to 1 in 230,000 [1].

The concentration of HPR and its variants was calculated using ε278  = 7446 M−1cm−1.

One measure of neutrality for mtDNA variants was calculated by comparing the number of non synonymous substitutions (dN) to the number of synonymous substitutions (dS) in each group.

The allele frequency of the variants was calculated as reads of alternate base/total reads.

The association of serum adiponectin concentration with genetic variants was calculated using a multivariate linear regression model.