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Services provider of genomics near Montpellier, France

Discover genomics services in wet lab, near Montpellier, France

GENXMAP is a genotyping service provider that is conveniently located near the city of Montpellier. Montpellier is a prominent city in France, celebrated for its rich culture and economic importance. GENXMAP's close proximity to Montpellier ensures convenient access to its genotyping services for local researchers, scientists, and institutions in Montpellier and the surrounding areas. This geographical advantage fosters seamless collaboration and enables easy access to GENXMAP's extensive range of genotyping methods and expertise for research projects and initiatives situated in and around Montpellier.

Let our wet lab services Genxmap to do the best for your genomics in Montpellier

Genotyping is the precise identification of a specific gene within the entire genome. It encompasses a wide array of methods and applications, ranging from detecting whole gene modifications to pinpointing single nucleotide polymorphisms (SNPs). GENXMAP, located conveniently near Montpellier, offers various genotyping techniques:

Gene Modification Detection: Genetic insertions or deletions can occur naturally or be deliberately induced through genetic engineering. This allows for monitoring changes in the function of specific genes. PCR, qPCR, and sequencing techniques are employed to identify these modifications, whether they occur on specific genes or across the entire genome.

Single Nucleotide Polymorphism (SNP) Identification: SNPs are common substitutions of individual nucleotides in the genome. These variations can either be inconsequential or have implications for pathological conditions such as autoimmune disorders, cancer development, or the body's response to pathogens, drugs, or vaccines. Identifying SNPs is crucial for the advancement of personalized medicine and clinical research. GENXMAP provides SNP genotyping through techniques like Taqman assay, rhAmp assay, or genotyping by Sanger sequencing or next-generation sequencing, chosen based on the project's objectives.

Copy Number Variation (CNV) Analysis: Taqman assay or the SYBR Green method are used to detect variations in the number of copies of specific genes. Taqman assay offers highly precise and specific identification and quantification of thousands of potential genes across more than 30 species. On the other hand, SYBR Green is a versatile and cost-effective technique that allows for the rapid customization of primers for various applications.

Genotyping by Sequencing Service (GBS): This involves Sanger sequencing or target-specific next-generation sequencing. The modification in the target gene is identified and analyzed by designing primers, optimizing gene identification through PCR, and sequencing the purified PCR product. This process allows for the detection of insertions/deletions, SNPs via Sanger or NGS, and CNV detection via NGS. The choice between Sanger sequencing and NGS is made based on the specific objectives of the project.

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