Unlock the potential of your research with GENXMAP’s precision genotyping services. We offer a comprehensive range of genotyping solutions designed to meet the unique needs of your project, from detecting gene modifications to identifying single nucleotide polymorphisms (SNPs) and copy number variations (CNVs). Our expertise, combined with cutting-edge technology, ensures accurate and reliable results, enabling you to advance your research with confidence.

The GENXMAP Genotyping Workflow:

Initial Consultation: We begin with a detailed discussion to understand your project’s specific needs and goals.
Sample Quality Control: Upon receiving your samples, we conduct thorough quality checks to ensure they are suitable for genotyping.
Automated DNA Purification: High-quality DNA extraction is performed using automated systems to maintain consistency and purity.
DNA Quantification and Normalization: We accurately quantify and normalize DNA to ensure uniformity across samples, essential for reliable results.
Genotyping Execution: We perform the selected genotyping method—PCR, qPCR, or sequencing—with precision and care, tailored to your project’s requirements.
Comprehensive Data Analysis: Our bioinformatics team analyzes the data, providing you with actionable insights and ensuring the accuracy and relevance of the results.
Detailed Reporting: We deliver a comprehensive report that includes data interpretation, insights, and recommendations to support your research.

Our Genotyping Service Offerings:

1. Detection of Genetic Insertions and Deletions:

Service Overview: Monitor and analyze naturally occurring or engineered genetic modifications with high precision.
Applications: Gene function studies, genetic engineering validation, and more
Techniques: PCR, qPCR, and sequencing.

2. Single Nucleotide Polymorphism (SNP) Genotyping:

Service Overview: Identify and characterize SNPs that may impact disease susceptibility, drug response, or other critical biological functions.
Applications: Personalized medicine, clinical research, and pharmacogenomics.
Techniques: TaqMan assays, Sanger sequencing, and NGS.

3. Copy Number Variation (CNV) Analysis:

Service Overview: Precisely quantify gene copy numbers to uncover variations that may affect gene expression or phenotype.
Applications: Cancer research, genetic disorder studies, and evolutionary biology.
Techniques: TaqMan assay

Speed and Efficiency: Our streamlined processes and advanced technologies ensure quick turnaround times without compromising quality.
Scalable Services: Whether you have a single sample or a large cohort, we can scale our services to meet your needs efficiently.
Ongoing Support: We provide continuous support and consultation, from project initiation to final reporting, helping you navigate any challenges that may arise.

Cu stom Solutions: We understand that every project is unique. Our services are fully customizable, ensuring that the genotyping method we use aligns perfectly with your research goals.
Advanced Technology: We employ state-of-the-art techniques and platforms, including PCR, qPCR, Sanger sequencing, and next-generation sequencing (NGS), to provide precise and detailed genotyping data.
Expertise and Support: Our team of experienced geneticists and bioinformaticians will guide you through every step of the process, from sample preparation to data interpretation, ensuring you get the most out of your results.
Comprehensive Reporting: We provide clear, detailed reports that not only present the data but also offer in sights and recommendations to support your research objectives.