Advanced Genomics offers comprehensive cytogenetic and genomic services, developing custom molecular assays with either microarray or multiplex PCR configurations. We use Illumina for SNP genotyping, LOH and CNV studies, and gene expression analyses. In addition, Advanced Genomics provides genetic characterization and pathogen testing services of tissue samples and cell lines.

GenomNZ^TM is a DNA testing laboratory within AgResearch Ltd. We provide research and product development solutions as well as commercial testing, to the agriculture, aquaculture and plant industries. We are able to sequence, assemble and discover SNP or microsatellite markers with our bioinformatics scientists, and have platforms to run assays developed from these markers.

Ambry Genetics is your partner for genomic solutions. We offer client specific, cost effective, pharmacogenomic services focusing on Next Generation Sequencing, Genotyping, and Gene Expression Profiling. Ambry Genetics is a CAP-accredited, CLIA-approved, GLP-compliant laboratory. For more information or to request a quote, contact Ambry Genetics at 949-900-5500 or visit www.ambrygen.com.

Australian Genome Research Facility Ltd (AGRF) is Australia’s largest genomics services provider with state-of-the-art service laboratory facilities in Adelaide, Brisbane, Melbourne, Perth and Sydney. Services provided include Sanger and next-generation sequencing, genotyping/SNP analysis, gene expression studies and nucleic acid extractions. AGRF is accredited to the internationally recognised ISO 17025:2005 quality standard as well as other regulatory licences.

BaseClear is the leading service providing laboratory for DNA-based services and research in the Benelux region. For all areas in which DNA plays a key role, BaseClear offers high quality services which can be customised to match your specific needs. BaseClear offers a comprehensive set of genome and transcriptome sequencing services, including project design, sequencing and complete downstream Bioinformatics analysis of the sequence data produced using the Illumina sequencing platform. Additionally BaseClear is currently working together with both the Belgian Bioinformatics company BioXpr and genomics software provider CLCBio to further improve the services which we provide to our customers.

Beckman Coulter Genomics exemplifies the combined experience and expertise of genomic service industry leaders Agencourt BioScience and Cogenics. With solutions for DNA Sequencing, Genotyping, Gene Expression and Biologics Testing, Beckman Coulter Genomics leverages the strengths of multiple technologies to meet the unique needs of each research experiment.

BGI-Hong Kong, as an affiliate of BGI, has established partnerships and collaborations worldwide, supporting a variety of researches and applications in disease, agriculture, environment, etc. The goal is to make leading-edge genomic science highly accessible to global research community and to accelerate biotechnology innovation and development.

BGI was founded in 1999 for the Human Genome Project. It has become the largest genomics organization in the world with a focus on research and application in personalized healthcare, agriculture, conservation and bio-energy fields. Based on large-scale sequencing, efficient bioinformatics, and innovative research initiatives, BGI has made great contribution to genomics development.

The Biopolis Shared Facilities (BSF) was established by the Agency for Science, Technology and Research (A*STAR) to support R&D needs for the biomedical and scientific community by centralizing resources and services. The Microarray Facility offers researchers the place to generate and incorporate genomic and expression microarray data into their researches.

Cambridge Genomic Services (Department of Pathology, University of Cambridge) has received Illumina CSPro status for gene expression profiling. The facility also offers SNP genotyping, Methylation and miRNA analysis. The high-quality service provides access to the latest technology, high quality experimental and quality control procedures, expertise in experimental design and bespoke bioinformatic data analysis solutions. The facility operates on a cost-recovery basis.

Cincinnati Children’s Cytogenetics Laboratory is a CAP-accredited CLIA-certified clinical laboratory offering Microarray services to detect DNA copy number changes. Our knowledgeable and experienced team provides two service options for multiple sample types: Tech Only with data generation or Full Service with data generation and comprehensive cytogenetic copy number data interpretation.

Cofactor is a full-service Next-Gen Sequencing Boutique providing solutions from experimental design to library-prep, sequencing, custom data analysis and visualization. Take advantage of our core team's depth of experience built on years of sequencing technology development work at a genome center. Visit our website to see our innovative pricing menu without logging in or contacting a sales representative.

At the Covance Genomics Laboratory, we go beyond transforming samples into data—we deliver science.
Using highly robust, automated processing protocols, we offer a wide range of leading edge molecular profiling services to enable drug discovery to meet your research goals. Our comprehensive services span sample processing to data delivery.

Since it's foundation in 1995, DNA LandMarks has been a world leader in agricultural genomics. Today we provide cutting edge DNA marker technology services to animal and plant breeders around the world. From marker development to mapping to high throughput screening and whole genome selection, DNA LandMarks provides fast competitive services to the agricultural breeding industry.

DNA Link, Inc. is a contract research service provider of genomics studies since 2000. The service expertise of DNA Link spans microarrays and next-generation sequencing, as well as personal genomics. DNA Link is an emerging leader in medical genetics research that is focused on establishing strong alliances with major hospitals to perform research on the genetic basis of common diseases. You could get the best quality, cost effective, fast turn-around time service from DNA Link.

DNAVision provides a full range of services in genetics and genomics for both research and regulated projects, from biomarker/trait discovery and validation to routine analysis. Using multiple platforms in a high quality environment (ISO 17025, GLP, GMP compliant), DNAVision's services include DNA/RNA extraction, genotyping, expression profiling and sequencing, including next generation sequencing.

Expression Analysis provides whole genome to focused set gene expression and genotyping assays along with DNA sequencings services, sequence enrichment technologies and bioinformatics support. Expression Analysis offers solutions for challenging specimens such as whole blood and FFPE tissues and nucleic acid isolation. Our quality system follows CLSI guidelines and our CLIA-registered laboratory supports GLP compliance.

GATC Biotech is Europe’s leading service provider of DNA sequencing and bioinformatics for industry and academic research. For nearly two decades we have been continuously developing new and comprehensive solutions for DNA sequencing and bioinformatics sequence analysis – for individual DNA samples through to complete genome projects. With a total of eleven sequencing instruments GATC has the largest commercially available sequencing capacity in Europe with two terabases per year. With over 100 employees the company serves over 10,000 customers in 40 countries around the globe and has subsidiary companies in Great Britain, France and Sweden.

Genes Diffusion offers breeding facilities for several animals and provides custom molecular assays. We use a wide range of Biomolecular technologies (qPCR, commercial and home-made microarray). Our platform based at the Pasteur Institute of Lille, has bioinformatics resources essential for data analysis from genomic and transcriptomic studies (e.g. GWAS).

GeneSeek, a Neogen Company provides comprehensive research and product development solutions for the Agribusiness, Pharmaceutical and Biotechnology industries. Using state-of-the-art genomics, proteomics and informatics platforms, we provide our customers with synergistic mechanisms for contract research, applied genomics and clinical/veterinary diagnostic services.

Genetic Visions Inc. provides DNA testing services to dairy and beef cattle producers whose goal is to improve their herd genetics through DNA technologies. For over 20 years Genetic Visions Inc. has been a leader in applied research in cattle genetics and selection techniques, achieved through the production of high quality data.

GeneWorks is a leading Australian provider of Genome Analysis and Bioinformatics Services to the local and international genomics research community. GeneWorks’ focus is on providing its clients innovative professional services of the highest possible quality, allowing researchers to achieve their goals with maximum efficiency, reliability and confidentiality. GeneWorks has been ISO 9001 certified since December 2005 and became an Illumina CSPro partner in November 2009. GeneWorks also supplies Custom Oligonucleotides, proudly manufactured in Adelaide, and is a Distributor of complementary innovative leading edge equipment, reagents and consumables. In 2007 GeneWorks became the first organization in Australia to begin providing services using the Illumina Genome Analyzer platform. Now with over two years experience with the technology, we provide and support a wide and expanding range of sequencing applications including the latest sequence capture approaches, and can accommodate both small and large projects. We also provide sequence assembly and downstream data analysis services. Our business goal is to continue to expand our sequencing capacity and range of service delivery, integrating new technologies as they become available.

The goal of our service is to become a reference for the development of research projects that are dependent upon Illumina technology and to be competitive in the European scenario including possible participation to projects founded by the European Community. We feel that this goal can be accomplished due to the scientific competencies of our team and the expertise with Illumina Expression and Genotyping platforms.

LGC Genomics delivers an array of high quality and flexible genomic services and related products to a wide range of customers. Illumina HiSeq technology is deployed within our service lab for genome sequencing and re-sequencing; transcriptome analysis; small RNA / microRNA discovery and analysis; ChIP-seq applications and DNA methylation analysis.

MFT Services was incorporated in September of 2001 specifically to fill the market need for a high quality supplier of microarray services and solutions. Today, MFT Services is recognized as the market leader in microarray outsourcing for gene expression, genotyping and resequencing analysis. MFT Services provides experimental design consultation, biological sample preparation, sample processing and data/statistical analysis services to clients worldwide. MFT Services has taken a leadership role in establishing quality standards for microarray processing, analysis and data management.

NCGR, a non-profit research institute with extensive experience in Illumina DNA sequence data generation and analyses, provides sequencing, genotyping, and analysis services in a collaborative setting. Service offerings include whole-genome (including de novo), transcriptome, methylome, ChIP, smRNA, and exome (targeted or whole). Assistance with experimental design, custom data analysis, and visualization tools for de novo assembly, alignment, and variant detection are available. You can also contact us for Illumina genotyping services.

NTNU Genomics Resource Center is now a global CSPro provider offering researchers in Trondheim, Norway convenient access to Infinium Whole-Genome Genotyping and Direct Hyb Gene Expression services using Illumina’s powerful genetic analysis technologies.

PerkinElmer DNA Sequencing and Analysis Services provides scientists access to sequencing platforms and robust analysis and visualization software delivered through a Web-based private secure cloud computing environment for “anytime, anywhere” genomic data interpretation and analysis, all backed by PerkinElmer industry expertise and the highest quality standards. Our quick turnaround time, interactive program consultation and experimental design support lets you focus on your research and avoid the hassle and cost of building in-house capabilities.

Pfizer Animal Genetics, a business unit of Pfizer Animal Health, provides comprehensive research, product development, and commercial offerings for beef, dairy, and sheep producers globally. Having invested in state-of-the-art genomic platforms, informatics, and world-class scientists, we partner with independent researchers, industry partners, and our own proprietary R&D efforts to develop and deliver genomic solutions and services.

The Ramaciotti Centre is a leading high-throughput functional genomics service provider, offering expertise in next-generation sequencing and microarray technology. We produce data of the highest quality and pride ourselves on excellent, personalized customer service. Our professional team has many years of experience facilitating projects from design through to downstream analysis.
Please contact us for a competitive quote.

SABiosciences, a QIAGEN company, offers clients a complete solution for genomic and expression analysis that delivers robust and reproducible results. SABiosciences accepts and processes cell, tissue, biofluid or fixed samples and then provides either pathway-focused or genome-wide analysis yielding superior results for scientists.

Sequensys provides next-generation sequencing and Voila! data analysis services. We offer high quality results, fast turnaround time, and competitive pricing. We provide convenient calculators on our website to help determine how much sequencing is needed and to instantly generate a quote for your project.  Our sequencing packages include preparation and QC of libraries, sequencing, and Voila! data analysis.

With 18 years experience, SeqWright, a CLIA certified and GLP compliant facility, provides FDA, Clinical, and Research-level Genomic services to the Pharmaceutical, Biotechnology and Academic communities. Specializing in Next Generation Genomics, Sequencing, Expression Analysis and Molecular Biology services, SeqWright has earned a reputation for quality, technical expertise and a willingness to provide client-specific solutions.

We also offer a comprehensive portfolio of genomic products and other genomic services supported by the latest platforms and technologies including the Illumina Beadarray and many others. Our broad service portfolio allows us to offer our customers flexibility and a comprehensive, professional experience for gene discovery projects including next generation sequencing, genotyping, gene expression analysis, DNA/RNA extraction and whole genome amplification with high quality bioinformatics options. We believe that we go 'that extra mile' for our customers, providing a friendly service with excellent turnaround times and good value.

TraitGenetics GmbH is a specialist in the area of SNP marker development and analysis in plants. Large sets of validated SNP markers and arrays are available for many crop plants which can be used in our services and collaborative projects during the entire plant breeding process.

The Finnish DNA Microarray Centre provides a broad range of microarray and functional genomics services using Illumina's advanced technologies. From sample preparation to preliminary data analysis, we offer a variety of options to address your specific research needs.

The Bergen node of the Norwegian Microarray Consortium (NMC) is a core facility providing a wide range of genomic profiling services including global gene expression for many species and large-scale examination of custom SNPs (GoldenGate) and DNA copy number variation. Our profiling services enable researchers to access microarray analysis without having to get involved in the experimental procedures themselves.