Genotyping methods and solutions

Cutting-edge sequencing and microarray technologies for analyzing genetic variation

Genotyping

Genotyping allows scientists to explore genetic variants such as single nucleotide variants, copy number variants, and large structural changes in DNA. High-throughput genomic technologies such as next-generation sequencing (NGS) and microarrays can provide a deeper understanding of disease etiology on a molecular level.

With multiple genomic targets potentially contributing to disease, analysis requires flexibility and accuracy. Genotyping data analysis tools can analyze results for millions of markers and probes and detect sample outliers, providing insight into the functional consequences of genetic variation.

Introduction to Genotyping
Genome-Wide Genotyping

Interrogate variants across the entire genome to obtain the most comprehensive view of genomic variation.

Targeted Genotyping

Focus time and resources on genotyping variants in a specific genomic region of interest, often with higher coverage.

SNP and SNV Genotyping

Compare techniques for detecting single nucleotide polymorphisms and variants to determine which approach is best for your needs.

Copy Number Variation Analysis

Detect DNA copy number changes, as well as aberrant chromosome amplifications and deletions, relative to a reference genome.

Custom Genotyping

Screen large sample sets for novel genetic variants or species, or target regions of the genome relevant to your specific research interests.

High-Throughput Genotyping

Large-scale genotyping with microarrays can identify variants associated with disease risk in large cohorts or populations.

Scientists Discuss Genotyping Projects

 
Polygenic Risk Scores Could Become Useful Tools in the Physician's Toolbox
Polygenic Risk Scores Could Become Useful Tools in the Physician's Toolbox

Researchers perform large genome-wide association studies to identify disease-associated DNA risk loci and develop PRSs for clinical validation.

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Scaling Up Genotyping
Establishing and Scaling an Efficient Genotyping Facility

Learn how Prenetics scaled up their genotyping laboratory to increase capacity and serve their growing customer base.

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Direct-to-Consumer Genetic Testing Expands in Asia
Direct-to-Consumer Genetic Testing Expands in Asia

A joint-venture DTC company focuses on the large and growing South Korean market as an entry point into Southeast Asia.

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Precision Genomics

Learn how genomics is advancing precision medicine by helping to pinpoint the underlying causes of diseases, optimize treatments, and create better outcomes.

Genomics Scientist in Lab
Genotyping Plants and Animals
Plant and Animal Genotyping

Enhance the value of crops and herds with screening and discovery tools that aid in breeding decisions. Learn more about plant and animal genotyping.

Cancer Germline Mutation Studies
Cancer Germline Studies

Analyze germline mutations that predispose individuals to cancer using microarrays and NGS. Learn more about cancer germline mutation analysis.

Complex Disease Genomics
Complex Disease Genomics

Find out more about disease association studies, gene target identification, polygenic risk scores, and other research topics. Learn more about complex disease research.

Pharmacogenomics
Pills

Understand how variations in the human genome affect our response to medications. These insights may help maximize treatment benefits while reducing health care costs. Learn more about pharmacogenomics.

Genetic and Rare Diseases
Genetic and Rare Diseases

We're developing solutions to facilitate early detection and intervention for affected families. Learn more about genetic and rare diseases.

Cardiovascular Disease Research
Cardiovascular Genomics

Cardiac gene panels using NGS can help to detect variants associated with cardiomyopathy and other heart diseases. Learn more about cardiovascular genomics.

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Array and Library Prep Kit Selector
Array and Library Prep Kit Selector

Easily identify the best array or sequencing library prep kit based on project type, starting material, and method.

Find the Right Kit
Genomics Consortia
Genomics Consortia

Explore consortium-built products that support high-throughput, multiplex studies of diverse populations and complex diseases.

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NGS Technology
NGS Technology

With unprecedented throughput, scalability, and speed, NGS enables study of biological systems at a level never before possible.

Explore NGS
Genomic Wellness Insights
Genomic Wellness Insights

Imagene Labs uses Illumina microarray and LIMS solutions to analyze genetic variants linked to wellness.

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Microarray Technology
Microarray Technology

Find out how our high-density bead-based microarray technology delivers trusted quality and reproducible data for cost-effective genotyping.

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Microarray Solutions
Microarray Solutions

Access a comprehensive range of array-based techniques and solutions for genotyping and epigenetics studies.

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