Sentence examples for variants were single from inspiring English sources

Four hundred five of 1256 unique variants were single base deletions, which could not be called by Caveman or MuTect.

Except for two non-coding indels in SDHA and one in SDHC, all variants were single nucleotide polymorphisms (SNPs) involving base replacements.

Most of these variants were single-base indels within sequence regions consisting of repeats of one base, and therefore they most likely represent homopolymer errors introduced through 454 sequence reads (Balzer et al. 2011) that were used for the assembly of the reference genome (Nowrousian et al. 2010).

The most common DNA sequence variants are single nucleotide polymorphism (SNP).

Some of these variants are single nucleotide changes and others are haplotypes - alleles at multiple loci that are inherited together.

Many other studies have identified possible genetic variants that appear to affect the AO in HD patients; the most frequently identified variants are single nucleotide polymorphisms (SNPs) often of uncertain functional effect (32).

Homeolog sequence variants (HSVs) were single nucleotide polymorphisms (SNPs; 89%) and single nucleotide indels (SNIs 10%).

Of those, 54 variants in 71 subjects were single and heterozygous, while ten patients had two, five had three and three patients four variants each.

All of the common variants were known single nucleotide polymorphisms (SNPs) and none were associated with NTDs (P > 0.05;) (Supp. Table S3).

Of these 18,868,899 were single nucleotide variants (SNVs or SNPs), 815,805 insertions and 972,588 deletions.

The other STs were single locus variants of ST32 or ST33.