SNPs are becoming markers of choice for many breeding programs.
Simple sequence repeats (SSRs) are the markers of choice, especially when constructing genetic linkage maps for plants.
Genomewide linkage studies are tending toward the use of single-nucleotide polymorphisms (SNPs) as the markers of choice.
Short tandem repeats (STRs) are the markers of choice for purposes of human forensic identification because of their considerable degree of polymorphism.
The N1s and S2p photoelectron signals were the markers of choice for confirmation of insulin grafting on the surface of succinic acid-modified nHA-s and the presence of insulin-grafted nHA-I in the PLGA nanofibers.
Single nucleotide polymorphisms (SNPs) are the markers of choice for most high throughput genotyping applications because they are ubiquitous in eukaryotic genomes, cost-effective to assay using automated platforms, and because allele calling, data analysis and data-basing are straightforward due to their biallelic nature.
For the past two decades they have been the markers of choice in a wide range of forensic profiling, population genetics and wildlife-related research.
With the parallel developments of dense SNP marker maps and technologies for high-throughput SNP genotyping, SNPs have become the polymorphic genetic markers of choice for genetic association studies which aim at discovering the genetic background of different phenotypes.
Until recently, Simple Sequence Repeats (SSRs), also called microsatellites, have been the genetic markers of choice, because they are economical to score, have high allelic diversity, and are usually selectively neutral [1].
SNPs are also markers of choice for studying evolutionary processes [ 10].
Our markers of choice for this study were based on several important factors.
