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GENXMAP
GENXMAP
GENXMAP
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Genotyping

Decode genetic information with our genotyping service dedicated to advancing your research

Genotyping

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.

Accelerate Biomarker Discovery with GENXMAP

Accelerate Biomarker Discovery with GENXMAP

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.

Services_Transcriptomiques-Genxmap

Transcriptomics

Drylab-Genxmap

Expertise & Training

Multiomics-Genxmap

Packages

Genomiques-GENXMAP

Genomics

Other solutions

Precise and advanced services, cutting-edge technologies, and reliable analyses.
Our rigorous approach ensures detailed results, essential for your scientific discoveries and clinical applications.

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