EXCITING NEWS!

We’ve Acquired BioEcho Life Sciences! Explore Innovative Nucleic Acid Extraction Solutions:

Welcome To The Advanced Molecular Era

Admera Health supports preclinical development and offers research-grade Next-Generation Sequencing and bioinformatic services. We combine expert scientific support, advanced laboratory processes, stringent quality control measures, and proven quality project management to deliver superior service. All projects are handled with exceptional care, operating in a CLIA/CLEP and CAP accredited environment.

Admera Health provides individualized attention for DNA sequencing projects.
Admera Health offers exceptional RNA-seq services with flexibility and capability for high-throughput according to customers’ needs.
Admera Health offers single cell services utilizing 10x Genomics platform enabling the study of cellular heterogeneity and the discovery of rare cell populations.
Admera Health offers numerous next-generation sequencing (NGS) assays to explore complex epigenome modifications and regulation.
Admera Health’s dedicated team of expert bioinformaticians offer comprehensive data analysis services covering genomics, metagenomics, transcriptomics, and epigenomics.
Admera Health offers a quick and supportive team to reach your goals! We work with both individually-barcoded libraries or any pre-pooled libraries

The Admera Difference

Quality Results Quality Deliverables

State of The Art Technology

Lightning Fast Turnaround Time

Competitive Rates

Unmatched Customer Service

Testimonials

  • “Our lab has been searching for a reliable sequencing center for the past several years. After having mixed success with several providers, we began sequencing with Admera. Not only are they fast, friendly, and dependable, they seem to treat our samples as if they were their own. We have projects ranging from ancient DNA to human exome to massive amplicon sequencing. No matter our needs or project specifics, they produce consistent and excellent results for every sample we send. We couldn’t be more appreciative of their team!”

    Petrov Lab, Stanford University

  • "We have been working with Admera since 2016 on numerous projects. We are return customers because they are notably reliable and provide the fastest turn around time we could find. Their staff obviously care deeply about their work and have gone above and beyond on multiple occasions to ensure the highest quality results tailored to our specific needs.”

    Niamh O’Hara, Cornell Tech

  • “Admera Health provide professional Next Generation Sequencing services that are second to none. Quotes and consultation are top notch and the timeliness of the services are remarkable. Admera has produced publication quality data on every single project and this company will continue to get my business and referrals. Admera is a valuable partner of the Vaccine Development Center at WVU and you should use them for your next project!”

    F. Heath Damron, PhD, West Virginia University School of Medicine

  • “We have been working with custom sequencing companies at ILVO for +10y and have switched to Admera Health for NGS applications such as RNA-seq, amplicon sequencing, and WGS projects. “We are very happy with the clean data, fast turnaround times and price/quality. Whenever we had questions (quotes, technical or administrative), we had a fast, professional answer and follow-up from support.”

    Steve Baeyen, ILVO

  • “Admera Health were a pleasure to work with. They completed the library preparation, QC and sequencing extremely quickly and to a great quality. When we requested re-sequencing of some samples, as we wished for more data, they had the libraries on hand and we had the data in ours within two weeks of our request. This was over the Christmas holidays. Questions were always answered within the same day, and the staff were very helpful.”

    Caitlin Singleton, Aalborg University

  • “I have sent samples for sequencing to Admera and this worked out very well, thanks to very interactive and efficient contacts with both technical and administrative services and with a great quality and time effective sequencing service.”

    Bernard de Massy, Institut de Génétique Humaine