Genotyping
Decode genetic information with our genotyping service dedicated to advancing your research
50K+
Genotypes revealed annually
Characterize Your Sample Phenotypes with Our Genotyping Service
We offer genetic variation analysis, allowing you to link observed traits to specific genetic markers.
Our services include:
Detection of genetic modifications (insertions/deletions)
Identification of Single Nucleotide Polymorphisms (SNPs)
Copy Number Variation (CNV) analysis
With GENXMAP, you benefit from personalized support to translate your genetic data into actionable insights, accelerating your research in biomedicine, personalized medicine, and the development of new treatments. Our genotyping service is designed to provide reliable and precise data, tailored to the specific needs of each research or clinical project.
Why Choose GENXMAP?
✅ Scientific excellence grounded in advanced expertise in genomics and transcriptomics
✅ Flexible and modular workflows tailored to diverse research models and sample types
✅ Hypothesis-driven approach with full support from experimental design to data interpretation
✅ Cutting-edge technologies combined with rigorous quality standards for reproducible, high-impact results
✅ Extended bench capabilities — leverage GENXMAP as your trusted wet-lab and data analysis partner
Download our service flyer
Genetic Variation Characterization
Exceptional Genotyping Expertise. With the capacity to process over 1,000 samples per week, we deliver precise and reliable analyses to drive your research forward.
Copy Number Variation (CNV) Analysis
Obtain accurate analysis of Copy Number Variations to identify disease-associated genetic alterations, with reliable results and personalized support for medical research.
Genotyping of Single Nucleotide Polymorphisms (SNPs)
Identify and characterize SNPs that may influence disease susceptibility, drug response, or other key biological functions.
Applications: Personalized medicine, clinical research, and pharmacogenomics.
Techniques: TaqMan assays, Sanger sequencing, and NGS.
Detection of Genetic Insertions and Deletions
Accurately analyze natural or induced genetic modifications.
Applications: Gene function studies, validation of genetic modifications, and more.
Techniques: PCR, qPCR, and sequencing.
Our Go/No-Go processes allow you to track the progress of your project in real-time. At each stage, you validate the transition to the next, ensuring complete control and maximum transparency throughout the entire process.
Our optimized timelines ensure fast and efficient execution of each project while meeting your specific requirements. This system ensures proactive time management, minimizing delays and maximizing productivity to deliver results that align with your expectations.
Our tailored processes are designed to meet the unique needs of each project, offering flexibility and personalized follow-up. This system ensures rigorous control while delivering accurate results that align with your expectations.
Our detailed analyses guarantee reliable and in-depth results tailored to each study. With cutting-edge tools and proven methodologies, we provide a precise understanding of genetic data, while adhering to the highest standards of quality and scientific rigor.
GENXMAP,
your trusted partner
Efficient and traceable scientific workflows
Transparent and well-defined processes, ensuring you remain in control with complete confidence throughout your project.
