Sentence examples for control for variant from inspiring English sources

As a result, it provides more accurate probabilistic scores for calls compared to earlier solutions, and thereby offers improved quantitative control for variant filtering, based on expected precision.

It is imperative therefore that continued active surveillance and infection control measures for variant Creutzfeldt Jakob disease are continued into the future.

A significant difference was observed in the variant genotype frequencies of the XPD Lys751Gln polymorphism between the patients with CML and control group (for variant homozygous genotypes, OR = 2.37; 95% CI = 1.20 4.67; P value = 0.016 and for combined heterozygous and variant homozygous genotypes, OR = 1.72; 95% CI = 1.10 2.69; P value = 0.019).

A statistically significant difference was observed in the variant genotype frequencies of the XPD Lys751Gln polymorphism between the patients with CML and control group (for variant homozygous genotypes, OR = 2.37; 95% CI = 1.20 4.67; P value = 0.016 and for combined heterozygous and variant homozygous genotypes, OR = 1.72; 95% CI = 1.10 2.69; P value = 0.019).

Controlling for variants such as these will be critical during the design/implementation of phase II and III clinical trials.

Green et al. followed this up by sequencing exon 11 in 506 cases and in 1211 controls for variants that occurred only once.

As an additional quality control for our variant calls, we calculated the SNV concordance in pairwise comparisons for all twin pairs.

Positive controls for each variant were identified by sequencing peripheral blood DNA from 30 healthy individuals and included with each set of assays.

For this study, we combined the RAVEN experimentally verified regulatory variants with 9,500 background variants, matched by distance to the nearest TSS (100 control variants for each true positive variant).

Although the frequency of the variant genotype was numerically greater in exposed cases compared with exposed controls for both variants, this difference was not significant for either T2119C (2.5% versus 1.1%, OR = 2.17, 95% CI = 0.26 18.27, P = 0.5) or C3161G (3.8% versus 2.9%, OR = 1.34, 95% CI = 0.36 4.98, P = 0.7).

One control child was homozygous for variant 1, resulting in a minor allele frequency of 4%, (2/52 chromosomes).