Genomic information at the service of human health and its environment
Sequencing
GenoScreen's historical activity since 2001, Sanger sequencing is used in all fields and for a wide range of applications. It is the standard technique for sequencing DNA accurately and robustly. On our dedicated platform, we offer routine sequencing and, in addition, customised services with various levels of intervention and analysis.
Our Sanger sequencing platform
Equipped with ABI 3730XL capillary sequencers, our platform meets your one-off and regular sequencing needs from tubes, strips or 96-well plates containing your PCR products or vectors.
Molecular barcoding
Molecular barcoding is a technique for identifying and genetically characterising a sample by targeting a ubiquitous gene, often mitochondrial or chloroplast.
Applications:
- Identification of a species from an isolated sample (microorganism, animal or plant species)
- Comparison of several samples from the same species or closely related species
Services offered by GenoScreen
- DNA extraction from any type of matrix (optional)
- PCR amplification, sequencing and assignment of samples to databases (NCBI, BOLD, etc.)
- Construction of phylogenetic trees
- MLST typing and whole genome sequencing (WGS) to characterise the genome
- Solutions for complex matrices via metabarcoding
Discover our services in molecular barcoding
Additional Sanger services
Primer walking
This sequencing method is ideal for:
Principle
The use of several primers makes it possible to obtain overlapping sequences leading to the reconstitution of the complete product. A universal primer is used to sequence an insert, obtaining a fragment of the vector sequence and the beginning of the insert.
A specific primer can then be designed on the sequence obtained and used to obtain the rest of the sequence. If the sequence of interest is known, all the sequencing reactions can be carried out simultaneously. This service can be performed either in single or double reading.

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Mutation detection
Sanger sequencing can be adopted to verify
Principle
Among other applications, the mutation detection is used to monitor TILLING (Targeting Induced Local Lesions in Genomes) in plants, or to verify mutations in genes of interest.
We can design specific primers to target a mutation and compare it to a reference sequence provided for verification.
If several mutations/positions are to be verified in the same genome region, we can also produce a detailed variance report compared with a reference gene.
Molecular barcoding (DNA barcoding) is a molecular taxonomy technique used to identify and genetically characterise a sample from a ubiquitous gene, generally belonging to the ribosomal, mitochondrial or chloroplast genome (COI, 16S, rbcL, etc.).
DNA barcoding applications
DNA barcoding can be used to:
- Identify species from an isolated sample
- Compare several samples from the same species or closely related species (phylogeny)
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Identification by DNA barcoding
GenoScreen offers a complete molecular barcoding service and can handle your samples from DNA extraction onwards.
- Identification of isolated micro-organisms
- Identification of animal or plant species
For complex inital matrices (e.g. assemblies of bacterial populations), GenoScreen develops metabarcoding solutions using NGS amplicon sequencing to obtain screenings of samples: soil fauna, intestinal flora, coral reefs, etc.
GenoScreen is a major international player providing sequencing and genomic analysis services.
The company’s expertise is based on an unique experience in genomic analyses, the use of cutting-edge technologies and the development and supply of exclusive bioinformatics tools and R&D services. GenoScreen offers a very broad range of sequencing services, from the most basic to the most advanced.
Sanger sequencing
GenoScreen Sanger sequencing services can be adapted to any type of project: magnitudes, delays and production frequencies, for a reading between 100 and 1200 bp.
Next-generation sequencing
GenoScreen offers a complete range of Next Generation Sequencing (NGS) services updated with the latest technologies (Illumina, PacBio ...).
Since 2008, GenoScreen offers a full range of next-generation sequencing (NGS) services in application to genomes, metagenomes and transcriptomes.
GenoScreen has cutting-edge technical facilities, giving you access to the latest technologies (Illumina, PacBio, etc.).
GenoScreen - Services provided
- Whole-genome sequencing (WGS)
New sequencing technologies available at GenoScreen offer the opportunity to analyse the entire primary structure of an isolated organism genome, whether eukaryotic, prokaryotic or viral. The analysis of data obtained allows to precisely characterize and describe any type of organisation and thus responds to a large panel of research problems. - Metagenomics
Metagenomics molecular approaches allows to analyse a community of organisms as a whole and to study a complex ecological niche exhaustively: a powerful and innovative approach to characterize the genes and, therefore, the biological functions carried by these microbiomes. - Targeted sequencing
Targeted sequencing allows specific analysis of targeted genes (or gene regions) on many samples in parallel. With NGS sequencing on MiSeq®, NextSeq500® or Hiseq® platforms, multiple genes can be evaluated with a smaller data volume, which is easier to manage and analyse than WGS datas. - Transcriptomics
High-throughput transcriptome sequencing (RNA-seq) has revolutionised prokaryotic and eukaryotic organisms quantitative and qualitative analyses. It allows, in particular, to perform differential expression analyses. - Ready to load
For a cost effective and responsive offer, GenoScreen proposes "Ready to Load" sequencing services for a wide range of libraries: a real research accelerator giving the opportunity to perform on last generation technical platform with advanced expertise.
The GenoScreen's assets
- A full range of NGS services
- Expert analysis and advice on the design of each analysis
- Unique expertise in microbiology
- High-quality data
- Exclusive bioinformatics tools: assembly, annotation, SNP detection, etc.
- Guaranteed short delay time
Sanger sequencing is a well-proven, low-throughput analytical solution that is well suited to fragments of all sizes (100-1200 bp read length). GenoScreen’s Sanger sequencing services can be adapted to suit all types of project, regardless the size, delay time or frequency.
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Sanger sequencing applications
Despite the emergence of new generation technologies (NGS), Sanger sequencing remains a reference method in many fields thanks to its reliability and accuracy.
GenoScreen offer
Flexible and available, our teams carry out sequencing from sample preparation to data analysis. See our documentation below to find out more about our services and to prepare your sequencing request form.
Premium range
The Premium offers correspond to a complete and personalised analysis of samples:
- Adaptation of the protocol to GC-rich sequences
- Supply of universal primers
- Sequence reading up to 1200 bp
- Results sent within 24 to 48 hours
The Premium range gives you access to our hotline, by phone and email: expert scientific support for sequence profile analysis.
Workflow tailored to your needs
All our offers are open to different sample formats:
- tubes
- strips
- plates, complete or not
Our One-Shot Plus and Optimized offers include additional information:
- Signal optimisation
- Reduction of any backgroun noise
- Assignment of indeterminate bases
- A specific protocol for mutation detection
Additional analyses
GenoScreen offers a range of services to complement sequencing:
Economic range
All the quality and responsiveness of GenoScreen at a low price!
Using your own PCR product + primer mix or even the sequencing reaction you have produced, we can take your samples to a more advanced stage for an optimised price.
GenoScreen advantages
- Flexible sequencing offer that adapts to your needs
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Personalised monitoring of your projects
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Simple ordering system
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Monthly invoicing or prepaid account
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Free transport of your samples by a GenoScreen-approved operator
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Optimised protection of samples in Genobox

Molecular metagenomics is used to analyze a community of organisms as a whole; as such, it provides an exhaustive assessment of a complex ecological niche. It is a powerful, innovative approach for characterizing the genes and thus the biological functions in a given microbiome.
Metagenomics has many advantages:
- Removal of the bias associated with PCR approaches
- Culture-free analysis and direct sequencing of microorganisms
- The functional description of a whole ecosystem
Applications
Metagenomics and human health
Metagenomics and the environment
In credit to its very detailed analysis of microbial communities present in the natural environment, metagenomics can be applied to the analysis of water quality, the development of biofuels and agrochemical products, soil remediation and the development of new practices in agriculture and animal husbandry.
GenoScreen - Services provided
GenoScreen's assets
- A dedicated team of expert scientists for each project.
- Assistance with developing the experimental plan and the sequencing strategy.
- Massive whole metagenome sequencing capacity.
- Exclusive bioinformatics tools.
- Cutting-edge scientific expertise for data exploitation (specially in the field of microbiology).
News
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