Sentences with phrase «nucleotide polymorphisms data»

Estimating population divergence time and phylogeny from single ‐ nucleotide polymorphisms data with outgroup ascertainment bias Wang, Y. and R. Nielsen.

Estimating population divergence time and phylogeny from single ‐ nucleotide polymorphisms data with outgroup ascertainment bias.

Reconstituting the frequency spectrum of ascertained single - nucleotide polymorphism data.

Reconstituting the frequency spectrum of ascertained single - nucleotide polymorphism data Nielsen, R., M. J. Hubisz, and A. G. Clark.

Not exact matches

One of the tools, the SNP - Seek database, is designed to provide user - friendly access to a type of genetic marker called single nucleotide polymorphisms (SNPs) identified from this data.

Furthermore, the analysis of data on single - nucleotide polymorphisms, the main cause of difference between human beings, allows the prediction of phenotypic effects of a particular genetic variation.

Using these data, we built a genetic model that includes 150 single - nucleotide polymorphisms (SNPs) and found that it could predict EL with 77 % accuracy in an independent set of centenarians and controls.

In their study (1), Sebastiani et al. used a number of different genotyping platforms and neglected to perform data quality - control steps, which resulted in their reporting several false - positive single - nucleotide polymorphism (SNP) associations.

The short note, by Editor - in - Chief Bruce Alberts, acknowledged that the study's authors «used a number of different genotyping platforms and neglected to perform data - quality control steps, which resulted in their reporting several false - positive single - nucleotide polymorphism (SNP) associations.»

MyOPGP data has facilitated the development of important genomic platforms, such as single nucleotide polymorphism (SNP), oligo and methylation arrays.

The sequence data easily can be used to identify single nucleotide deletion, insertion, polymorphism and translocation and copy a number of changes on the DNA level.

Microsatellite genotypes were obtained for 203 clinical infection samples from eight locations, and Illumina paired - end sequences were obtained to yield high coverage genome - wide single nucleotide polymorphism (SNP) data for 65 clinical infection samples from four locations.

This technology can be applied to gene expression, SNPs (single nucleotide polymorphisms) and proteomics data to improve diagnostic and drug target identification and prioritization, predictive toxicology and drug screening.

One of the tools, the SNP - Seek database, is designed to provide user - friendly access to a type of genetic marker called single nucleotide polymorphisms (SNPs) identified from this data.

A previous method, COIL, was developed to estimate complexity of infection (COI) from single nucleotide polymorphism (SNP) data, but relies on monogenomic infections to estimate allele frequencies or requires external allele frequency data which may not available.