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:
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Detection of genetic modifications (insertions/deletions)
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Identification of Single Nucleotide Polymorphisms (SNPs)
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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.
Precision Genotyping, Unlocking Genetic Insights
GENXMAP, your trusted partner to support you in your research.
Service Details
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Project Objectives Analysis
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Selection of the Most Appropriate Genotyping Method (Technology and Type of Analysis).
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Project Objectives Definition:
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Identification of specific targets (genes, genomic regions, mutations).
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Selection of the appropriate method (Conventional PCR, qPCR, Multiplex PCR, Digital PCR).
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Primer and Probe Design:
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In silico design and validation of primers to ensure specificity and efficiency.
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Option to use fluorescent probes (e.g., TaqMan) for quantitative PCR.
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PCR Protocol Optimization:
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Adjustment of primer and enzyme concentrations.
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Testing hybridization temperatures and cycling conditions to maximize sensitivity and specificity.
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Performance evaluation on test samples.
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Validation and Quality Control:
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Implementation of positive and negative controls for each reaction.
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Validation on different sample types to assess robustness and reproducibility.
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Result Analysis:
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Interpretation of capillary electrophoresis results (visualization of PCR amplicon products).
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Generation of detailed reports of the optimized protocol.
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PCR Development Validation with the Client.
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Data Provided in Standard File Formats (e.g., PDF, Excel, FASTQ, VCF).
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Technical Support for Interpretation or Integration into Other Analyses.
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Optimized and Transparent Services
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.
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+50 000 Genotypes Revealed Annually
Exceptional Genotyping Expertise
With our ability to process over 1,000 samples per week, we guarantee precise and reliable analyses to advance your research projects.
Genetic Insertion and Deletion Detection
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Analyze Natural or Induced Genetic Modifications with High Precision.
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Applications: Gene Function Studies, Validation of Genetic Manipulations, and More.
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Techniques: PCR, qPCR, and Sequencing.
Genotyping of Single Nucleotide Polymorphisms (SNPs)
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Identify and Characterize SNPs That May Influence Disease Susceptibility, Drug Response, or Other Important Biological Functions.
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Applications: Personalized Medicine, Clinical Research, and Pharmacogenomics.
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Techniques: TaqMan Assays, Sanger Sequencing, and NGS.
Analyse des Variations du Nombre de Copies (CNV)
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Get Accurate Copy Number Variation (CNV) Analysis to Identify Genetic Alterations Linked to Diseases, with Reliable Results and Personalized Support for Medical Research.