The Genomics group at Corteva Agriscience™ is a certified provider with a focus in agricultural genomics and extensive experience in a wide range of plants and animals.

Please contact Victor Llaca directly at sequencing@corteva.com.

Histogenetics is applying cutting-edge sequencing technologies to study all living species, helping lead innovation in human, plant, and animal research and precision medicine.

The French Resources Centre for Plant Genomics (CNRGV) is a national infrastructure belonging to the French National Research Institute for Agriculture, food and Environment (INRAE). Settled in Toulouse (France) in 2004, the CNRGV is both a Biological Resources Centre (BRC) dedicated to all plant genomic resources and a service provider for plant genomics projects.

It aims at providing innovative and efficient genomic tools to better characterize plant biodiversity and understand how plants adapt to their environment through the analysis of their genomes.

Its field of expertise includes the development of HMW DNA extraction protocols dedicated to plants, targeted sequencing of genomic regions of interest and plant genomes analysis based on genome optical mapping combined with genomic sequences (produced in collaboration with sequencing facilities). The CNRGV has also developed bioinformatics expertise to analyse and explore the complex structures of plant genomes.

The CNRGV has implemented the Bionano Genomics optical map platform in 2016 and produced optical maps for more than 120 different plant species.

Gentyane is a platform offering Genomic services at INRAe Clermont-Ferrand. We intend to provide robust and new release technologies for  a complete genomic approach.

We carry out research and development activities using long reads sequencing, genotyping and optical mapping technologies.

Whether you are public or private, whether your project is low or high throughput, we will provide the most suitable strategy to answer your needs.

The McDonnell Genome Institute (MGI) has a rich 25-year history in the world of genomics. From contributing approximately 25% of the human genome reference to sequencing the first cancer tumor/normal pair to generating sequences for multiple de novo plants, animals, and microbiomes, MGI has become a scientific leader in this field. Through strong collaborative relationships, MGI continually develops and refines genomic-based tools for the future of science

MGI offers the entire Saphyr System workflow from samples to analysis allowing scientists to assemble genome de novo as well as detect novel structural variants. Please contact MGI directly at mgi@wustl.edu.

CLIA and CAP certified, Praxis Genomics, provides a solution for those who could not get a genetic diagnosis with traditional cytogenetic, microarray and exome sequencing approaches. They provide genetic testing with unsurpassed sensitivity and specificity based on combination of Bionano technology and traditional short read Illumina sequencing of DNA and RNA.

Carrier testing that investigates the entire genome and is not part of currently available panels can be performed for couples with reproductive difficulties and for individuals who want to have a clear understanding of any family predisposition for the development of cancer or neurodegenerative disorders.

Genetic consulting and counseling services are provided to assist our customers in selecting the appropriate test combination and to explain the clinical significance of the results in a clear and concise manner.