Sentence examples for variants that represent from inspiring English sources
Vulin, C., Leimer, N., Huemer, M., Ackermann, M. & Zinkernagel, A. S. Prolonged bacterial lag time results in small colony variants that represent a sub-population of persisters.
Only common variants that represent or are in strong linkage disequilibrium (LD) with previously-identified signals at established loci reached traditional thresholds for exome-wide significance (P < 5.0 × 10 - 7).
The following innocuous sequence variants that represent known single nucleotide polymorphisms (SNPs) were found: P15S; SNP rs3802829 was found in seven patients A404V; SNP rs36111323 was found in seven additional patients.
The panel of strains included fHBP variants that represent approximately 70% of the variants that caused disease in these populations.
MU2A annotates sequence variants for every SNP position and provides allele frequencies, simplifying the identification of sequence variants that represent minor alleles.
Although our sample set was selected for certain mutations, our specimens contained variants that represent the full spectrum of mutations that are identified in NSCLC and CRC specimens.
With this technology we were able to identify and quantify variants that represented as little as 0.05% of the HIV-1 quasispecies.
These cut-off values were also dependent on the number of reads, but resistance mutations that represented on average 0.05% (range 0.014 0.29%) and viral variants that represented on average 0.11% (range 0.09 0.21%) were high-confidence, i.e. exceeded our statistically derived cut-off values.
After excluding known germline variants, there were 24 nucleotide variants that represented potential somatic mutations.
Only specific sequence variants that represented more than 3% of the total population for each reference miRNA were considered biologically relevant.
These findings show the power of TNGS in identifying sequence variations in a very large gene and the surprising results obtained in this study greatly expand the catalog of known VDR sequence variants that may represent an important clue in the emergence of vitamin D deficiency.
