Service Providers

The Genomic Platform sets up high-throughput technologies to support the characterization of genomes from different points of view, through molecular biology techniques to bioinformatics analyses. Their services include basic PCRs and qPCRs, array based assays, high-throughput sequencing, and bioinformatics.

The functional genomics core at IDIBAPS allows researchers access to advanced technologies and protocols to study and analyze genomics and single-cell transcriptomes. Services range from quantitative and qualitative analysis of nucleic acids to the execution of more complex projects including library synthesis and sequencing.

The HIMC offers genomics services for human and mouse immunology-related projects: RNA, cfRNA/Exosome, genomic DNA, and cfDNA extraction; Bioanalyzer and qubit analysis services.

The DNA Technologies and Expression Analysis Core at the Genome Center enables access to high throughput genome-wide analyses at economical recharge rates, as a functional extension of your laboratory.

Cambridge Genomic Services (CGS) is a service provider offering a wide range of assays covering sequencing platforms and microarray. We are experts in experimental design, sample processing and bioinformatic analysis for Illumina and Nanopore based sequencing, for all types of assays covering DNA, RNA and single cell. We are also very experienced in array-based technologies for genotyping and methylation. Whatever your needs, we will have a solution for you.

The UMGC provides genomic technologies and services to researchers and clinicians at the University of Minnesota and to academic and industry scientists throughout the U.S. and internationally. We strive to keep pace with the ever-broadening world of “omics” technologies and to expand our role at the University and the wider biotech community.

The One Health Innovation Core Lab at OSU is conducting cutting-edge genomic research to further advancements in both human and animal medicine. They offer a host of Illumina sequencing services, from small whole-genomes, targeted genes, and transcriptomics, plus single cell sequencing from Parse Biosciences.

The Virus Characterization, Isolation, Production and Sequencing Core provides services to TNPRC, Tulane University, and affiliate investigators. The VCIPS core is divided into two primary components: 1) Virus characterization, isolation, and production and 2) Next generation sequencing.

Polo di Innovazione Genetica e Biologia Genomica is a health-tech company, a model for research and service provision in the fields of genomics, bioinformatics, medical genetics, ecology and population genetics. The Genomics and Bioinformatics laboratory, based in Siena (Tuscany), supports life science research with library preparation, single-cell RNA sequencing and other genomics and transcriptomics services for researchers.

The CNIC Genomics Unit is dedicated to providing advanced and high-quality genomics technology and support to the scientific community through its next generation sequencing technologies. They provide in-depth support for every sequencing project, including project consultation, sample quality control, sample library preparation, and data generation.

The Nextgen Sequencing/Genomics Core facility at Texas Tech’s Center for Biotechnology and Genomics provides a range of single cell sequencing services, including library preparation from DNA/RNA and data analysis. They also provide student training in Nextgen sequencing and associated Bioinformatics.

The Genomics Core Technology Unit (GCTU) at Queen’s University Belfast is a state-of-the-art sequencing facility providing access to advanced genomic services and expertise to support cutting-edge research. The GCTU offers a wide range of services including next-generation sequencing, single cell sample preparation and analysis, and bioinformatics, enabling researchers to conduct high-quality genomic studies.

The CGC’s mission is to bring the newest next generation sequencing (NGS) technologies to the research community and to help facilitate cutting-edge cancer research in the Texas Medical Center and other areas of Texas. The CGC offers the bulk DNA sequencings, the bulk RNA sequencings and single-cell RNA sequencings.

The Genome Sequencing Facility (GSF) at Greehey Children’s Cancer Research Institute (Greehey CCRI) at UT Health San Antonio (UTHSA) utilizes state-of-the-art technology, including Parse Biosciences’ single cell platform, to generate high-quality genomic data and provides support with its analysis.

The Center for Biomedical Research Support (CBRS) provides access to cutting-edge technology, including the Parse Biosciences single cell platform, and expert advice to enhance research.

The SAGC provides a broad range of services including single cell and spatial transcriptomics, bulk RNA sequencing, small RNA sequencing, exome and genome sequencing, epigenomics, metagenomics and a range of other custom methods.

The Gene Expression Center provides cost-effective, cutting edge transcriptomic (bulk, single cell & spatial transcriptomic) and large scale genotyping/methylation services to the University of Wisconsin campus as well as colleagues at public and private institutions.

NUSeq serves scientists on both the Chicago and Evanston campuses, as well as those at external academic and commercial organizations and offers single cell RNA sequencing using the Parse platform.

Within the Genomics Core, DNA sequencing supports research across the campus and extends to projects in collaboration with other institutions, including the sequencing of genomes, single cell RNASeq, ChIPSeq, methylSeq, metagenomics and other applications.

The Genomics Core at Cedars-Sinai Medical Center offers new applications, such as single-cell RNA sequencing, microbiome profiling and targeted transcriptome resequencing for FFPE samples, using a brand-new Illumina Novaseq, MiSeq and NextSeq.

The Genomics Research and Technology Hub (GRT Hub) is a core research facility that provides emerging nucleic acid technologies to UCI and provides genome-wide analysis for clients interested in gene expression, regulation of gene expression, and genome sequence and variation.

The Faculty of Medicine and Dentistry (FoMD) Advanced Cell Exploration (ACE) Unit is a multi-user core facility at the University of Alberta. It offers a number of different services including assistance in experimental design and troubleshooting, single cell sequencing and data processing, NGS, PCR, among others.

Single Cell Discoveries specializes in innovative single-cell sequencing technologies, multi-omic applications, and spatial transcriptomics. Single Cell Discoveries delivers high-impact insights to biopharmaceutical companies, healthcare systems, and academic research centers worldwide. Single Cell Discoveries’ mission is to accelerate groundbreaking research by developing and providing state-of-the-art single-cell technologies as a service.

The Genomics & Cell Characterization Core Facility supports life sciences research with sequencing, library prep, single cell, and other services for researchers within and external to the University of Oregon.

Our skilled scientists have refined protocols to efficiently dissociate cells and nuclei from a range of tissue samples such as brain tissues, tumors, and organoids.

The Princess Margaret Genomics Centre serves local, national and international clients from both academic and commercial research organizations.