Sentence examples for variants were generally from inspiring English sources

Since the variants were generally common in current populations, they will likely prove useful for validating expression differences across multiple tissues, populations and enhancing our understanding of the differential predisposition to common diseases and variation in drug responses in different ethnic groups.

Variants were generally streak-plate cultured at 37°C on Bolton or Blood agar in vented GasPak jars in a microaerobic environment generated by atmosphere evacuation, followed by equilibration with a gas mixture of 80% N2, 10% CO2, and 10% H2.

Variants were generally called with high accuracy, however identification of SNPs (single-nucleotide polymorphisms) was less accurate for high damage/low divergence samples.

Because all 100 subpopulations evolved from the same progenitor population, the common variants were generally the same between subpopulations, allowing SNP sets to be created from the n = 1000 samples.

All peptides explored were observed to form cross-β amyloid fibrils by TEM, and X-ray FD as previously described.[ 16] K/A variants were generally narrow filaments, whilst K/R variants formed laterally associated structures that appeared to be more crystalline in appearance.

Indeed, these alleles did not show a consistent frequency among the amplicons in all individuals that seem to carry these variants, were generally associated with low number of reads, and for a number of individuals these alleles were completely absent in one of the amplicon replicates.

Events in somatic assembly and maturation of antibodies such as hypermutations and rearrangement of variable loops (CDRs — complementary determining regions) and selection among a wide range of framework variants are generally considered to be random processes.

These spinal variants are generally easier to appreciate on radiographs or CT than on magnet resonance imaging (MRI) [1, 8].

[2], [3] The effect of more common variants is generally much less potent than that of rare variants, and as a result, for example, not all carriers of ABCC8 variants develop diabetes.

Rare (MAF < 0.01) variants are generally not well imputed by either low or high density arrays.

Such variants are generally not directly identifiable through GWAS because of incomplete SNP tagging.