Genomics & Bioinformatics
Admera Health is providing Next Generation Sequencing
solutions to researchers worldwide.
Admera Health is providing Next Generation
Sequencing solutions to researchers worldwide.
Our Genomics and Bioinformatics Services gives comprehensive support from the initial project consultation and continues even beyond completion of project. Our facilities have all the latest equipment and instruments to facilitate your requirements.
Learn more about Admera Health’s Next Generation Sequencing solutions:
Providing comprehensive, affordable, and creative solutions in DNA research of human, non-human and microbial samples for scientists. Admera Health offers the latest technology in next-generation sequencing and an experienced, high-quality project management team to guide you every step of the way.
RNA-seq is a powerful tool for analyzing gene expression levels within an individual sample as well as for comparing differential gene expression between multiple samples. RNA-seq can detect the presence of novel isoforms, alternatively spliced transcripts; potential gene fusion events can also be detected through analysis of RNA-seq data. Admera Heath offers a complete solution from RNA extraction to bioinformatics analysis.
Researchers looking for sequencing only solutions will find that Admera Health offers a quick and supportive team to reach your goals. Admera Health works with both individually-barcoded libraries or any pre-pooled libraries.
Upon receipt of your samples, Admera Health performs comprehensive quality control steps which are detailed in reports that are sent to you within 24 hours. Our QC entails Qubit, Tapestation, and qPCR.
Admera Health Bioinformatics team empowers researchers with informative results with ready to review reports along with expert support. Admera Health’s accomplished bioinformaticians provides comprehensive support and customized solutions to enhance the effectiveness of our customers’ research.
- Next Generation Sequencing (NGS) and microarray data processing, analysis and interpretation
- Bioinformatics data mining and integration
- Statistical analysis and modeling
- Machine learning and AI method development and applications
- Function, pathway and network analysis
- Genome and disease annotation
- Customized data structure and algorithm development
- Bioinformatics consulting
Bioinformatics team also has special expertise in Precision Medicine solution and Immuno-Oncology research, including neoantigen prediction, Immune Repertoire (TCR/BCR) analysis etc.
Researchers who are investigating a specific set of targets will find solutions with our expert team. Different methods can be employed based on your research requirements. As always, Admera Health will offer affordable and creative solutions.
Sample Collection & Preservation: Stool Sample
Our preservation tubes prevents bacterial growth and nuclease activity. The preservation solution can be stored in ambient temperature prior to extraction.
“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!”
“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.”
“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!”
“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.”
“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.”
“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.”