Genotyping is the process of determining the DNA sequence, called a genotype, at specific positions within the genome of an individual. Sequence variations can be used as markers in linkage and association studies to determine genes relevant to specific traits or disease.
Each species is defined by a distinct set of common characteristics, but even within a species, there are subtle differences among individuals. In the human species, we can easily spot physical differences such as hair color or eye color among people, but every species has differences among individuals, even those considered non-living, such as viruses. Though the differences are not drastic enough to be called out as a distinct species, individuals within a species that do have slightly different characteristics are called variants.
Variation is the term used to describe the characteristic that is different within a populations of distinct individuals within a single species. For example, some populations of soybean plants will have resistance to a common fungal pathogen such as phytophthora root rot; whereas, other populations will be susceptible to this pathogen. In simplistic terms, fungal resistance is a variation. The phytophthora root rot resistant population has some sort of change enabling the plants to defend themselves against the fungus. If the fungal resistance is passed onto subsequent generations of plants, the change is most likely in the genome.
Environmental and genetic differences are at the root of these visible or phenotypic changes. Since environmental changes are not heritable, most researchers are interested in studying the genetic variation that results in the physical differences. Genetic variation can be passed to the next generation, and can increase the fitness for species.
Genotyping is the experimental procedure that identifies the differences in DNA sequence among individuals or populations. The genotype is used to understand the connection between genotypes and phenotypes. An individual genome is identified as a distinct variant when compared to a reference sequence, which is derived from the general population or a defined subgroup. A variant sequence can differ from the reference sequence in numerous ways. Types of genetic variation include single nucleotide variants (SNV), single nucleotide polymorphisms (SNPs), insertions and deletions (indels), and copy number variation (CNV).
SNPs are the most common type of sequence variant investigated by researchers; they are typically defined as SNVs that occur at >1% in the population. Based on the number of SNPs cataloged in Build 151 (Oct 6, 2017) of the SNP database, dbSNP, maintained by the National Center for Biotechnology
Information (NCBI) (RefSNP count 660,773,127)  and a haploid genome size of 3.1 x 109 bp , the human genome should contain a SNP approximately once every 9.5 bases! Other common model organisms show a similarly high
frequency of SNPs .
By comparing genetic variations among individuals of a species, researchers can identify heritable genetic signatures, or markers, relevant to specific traits. These unique differences can be used as markers in linkage and association studies.
Genome-wide association studies, or GWAS, compares genetic differences across entire genomes from two individuals or populations. For example, the genomes of a group of people that have a disease can be compared to a genomic sequences from a similar group of people without the disease. Any SNP or haplotype that is more prevalent in those with the disease is called an associated genetic marker.
Association is merely the beginning, and many studies are needed to confirm if the genetic variation is truly the underlying genetic change that codes for the variant or trait. The National Center for Biotechnology Information (NCBI) maintains a registry of human genomic variations and their relationship to health called ClinVar. The website archives variation in human genes, and the evidence supporting the association to a particular phenotype. Besides human health, finding the relationship of genotype to phenotype has many applications:
There are varied approaches to SNP genotyping depending on the number of samples, the number of genotypes to be tested, and the amount of sample material available, all factoring into the choice of technology.
High-throughput genotyping methods include whole genome analysis by NGS, SNP analysis using microarrays, and targeted sequencing methods such as amplicon sequencing or hybridization capture technology.
Low-throughput analyses include using multiplex quantitative PCR (qPCR), PACE™ (PCR Allele Competitive Extension) SNP genotyping, and multiplex digital PCR (dPCR) to identify the genotype of a specific SNP.
Learn more about the language used in genotyping studies.
Quantitative polymerase chain reaction (qPCR) is a commonly used genotyping technique. Often employing a primer-pair and target-specific fluorescent probe, qPCR can be a sensitive and specific way to identify SNPs. IDT offers a complete SNP genotyping solution with predesigned assays, as well as complementary easy- and ready-to-use reagent mixes. For other applications, modified probes are available that can be incorporated into custom qPCR assays.
Targeted sequencing uses deep sequencing to identify known and novel variants within your region of interest. Thus, it can be used as a method of gene expression analysis, mutation detection, gene structure analysis, and genotyping.
PACE SNP genotyping uses competitive, allele-specific PCR and a simple, easily detected fluorescent readout for bi-allelic genotyping. Obtain primer sets from IDT for cost-effective, high-throughput assays.
Digital PCR (dPCR) includes the same reagents found in a typical qPCR assay and amplified in a similar manner, but dPCR divides the reaction into nano-sized droplets or wells prior to amplification. The partitions are so small that either 1 or 0 templates are in each. After amplification, the fluorescence in the well or droplet represents the genotype.
For user-defined methods, order custom probes with modifications, such as Affinity Plus™ qPCR locked nucleic acid probes, that increase probe stability and enable designs within difficult sequences and with selective target identification.
The rhAmpSeq™ system enables highly accurate amplicon sequencing on Illumina® next generation sequencing (NGS) platforms. Whether you are investigating thousands of targets or a few, the fast and easy rhAmpSeq workflow generates NGS-ready amplicon libraries for deep, targeted resequencing.
Use Affinity Plus™ qPCR Probes for SNP genotyping, transcript variant identification, and more sensitive target detection in challenging samples (FFPE tissue, biofluids). The Affinity Plus bases used in these qPCR probes are locked nucleic acid monomers. When incorporated into a probe, they impart heightened structural stability, leading to increased hybridization melt temperature (Tm).
PACE™ SNP genotyping uses competitive, allele-specific PCR and a simple, easily detected fluorescent readout for bi-allelic genotyping. Obtain primer sets from IDT for cost-effective, high-throughput assays.
The rhAmp SNP Genotyping System is a fully integrated genotyping solution that includes an extensive predesigned assay collection, a custom design tool, optimized reagent mixes, and optional synthetic control templates. SNP detection may be performed on any commonly available qPCR instrument.
Precise and easy-to-use, the rhAmp SNP Genotyping System offers an out-of-the-box solution for SNP genotyping studies for small discovery or large screening projects.
*RUO—For research use only. Not for use in diagnostic procedures. Unless otherwise agreed to in writing, IDT does not intend for these products to be used in clinical applications and does not warrant their fitness or suitability for any clinical diagnostic use. Purchaser is solely responsible for all decisions regarding the use of these products and any associated regulatory or legal obligations.