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Bioinformatics Analysis Services

Expert NGS data analysis for genomics, transcriptomics, metagenomics, and epigenomics that are customized to your research and delivered publication-ready.

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  • Capabilities

  • Pricing

  • Turnaround Time

  • Sample Submission Requirements

Comprehensive Bioinformatics Analysis Across All Major NGS Applications

  • Whole genome sequencing (WGS) variant detection and annotation, whole exome sequencing (WES) analysis, structural variation and CNV detection, low-pass WGS imputation and genotyping, tumor fraction estimation in cfDNA, host-vector insertion detection, PDX read cleaning

  • Bulk RNA-seq differential expression, single-cell RNA-seq (10x Genomics, Parse, Takara), spatial transcriptomics (Visium HD, STOmics/Stereo-seq), gene ontology and KEGG pathway analysis, alternative splicing, isoform quantification, gene fusion detection

  • Whole metagenome shotgun analysis, 16S and ITS amplicon profiling, de novo assembly and annotation, taxonomic classification and abundance, antimicrobial resistance gene detection, functional profiling, community diversity analysis

  • Whole genome bisulfite sequencing (WGBS), reduced representation bisulfite sequencing (RRBS), ATAC-seq chromatin accessibility analysis, ChIP-seq peak calling and annotation, methylation pattern analysis, differential methylation

  • Cell Ranger / Parse pipeline processing (QC, filtering, barcode counting, UMI deduplication), dimensionality reduction and clustering (PCA, UMAP, t-SNE), cell type annotation with marker gene identification, differential gene expression across clusters and conditions, VDJ clonotype analysis for TCR and BCR immune repertoire profiling, multi-sample integration and batch correction, pseudotime and trajectory analysis

  • Space Ranger and STOmics/Stereo-seq pipeline processing, tissue segmentation and spatial clustering, gene expression mapping and visualization, spatial deconvolution with scRNA-seq reference integration, spatially variable gene detection, cell-cell interaction analysis within tissue architecture

We Put Your Needs At The Center Of Everything We Do

Attentive Customer Service

  • 24 hour response times to all requests

  • Ph-D level project support

Quick Turnaround Times

  • Turnaround times as fast as 10 - 15 business days

  • Custom delivery timelines can be created as they’re needed

Quality Control

  • Admera Health maintains the regulatory thresholds required of a clinical lab, ensuring your sample is handled properly

  • Transparent QC requirements 

Bioinformatic Analysis

  • Our bioinformaticians provide data and insights to make your job easier

  • We provide an array of standard analyses, as well as more custom options

Project Customization

  • Our team works with you 1:1 to develop a project based on your specific needs

  • We're not limited by the restrictive processes of other NGS providers 

US-Based Operations

  • We perform all NGS solutions in South Plainfield, New Jersey

  • Your sample processing is efficient and secure with us

Sample Delivery Can Be Frustrating, So We Made It Easy

Click The Image To View Our Sample Delivery Guide

No more guesswork, frustration, or stress. Our sample delivery guidelines were designed with simple, straightforward directions to make this process easy for you.

Meet Your Research Goals With Our Expertise

Scientist-to-Scientist Support

  • 24 hour response times to all inquiries

  • Dedicated project scientist assigned to your study from kickoff through final delivery

  • PhD-level bioinformaticians collaborate directly with your research team on experimental design and pipeline customization

Quality Control & Accreditation

  • CLIA/CLEP-certified and CAP-accredited laboratory in South Plainfield, NJ

  • Multi-layer QC at every processing stage ensures your results withstand peer-review scrutiny

  • All analyses performed in-house at our US facility—your data never leaves the country

Publication-Ready Deliverables

  • Complete analysis reports with figures, supplementary tables, and methods sections ready for journal submission

  • Code and pipeline documentation provided upon request for full reproducibility

  • Data delivery via secure FTP or BaseSpace with clear download instructions

Don’t Just Take Our Word For It

  • “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!”

    Associate Professor & Director

    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.”

    Bioinformatician & Lab Manager

    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.”

    Postdoctoral Research Fellow

    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 great quality and time effective sequencing service.”

    Research Director

    Institut de Génétique Humaine

  • “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

  • “Since 2018, we have had the pleasure of collaborating with Admera Health. We utilize their custom services for WGS, ddRAD, RNA-seq, amplicon sequencing, and environmental DNA extraction. The latter method was specifically implemented to meet our needs. Admera provides cutting-edge technology and excellent customer service. Their project managers are communicative, responsive to inquiries, open to discussing results, and always seeking ways to improve project execution. Data quality is consistently high and turnaround time for results is rapid.”

    Researcher

    Bio Bureau Biotecnologia

  • “Overall, working with you all has been a delight. I was very impressed at how communicative and responsive Admera Health during the entire process. After analyzing my raw data, I was able to retain a large number of reads, too. I highly recommend you all to other colleagues getting started in genomics like I have.”

    Researcher

    Texas Tech University

  • “As always, working with Admera Health was a pleasure. My dissertation has relied on their services and has taken a weight off because they always deliver quality RAD-seq results in a timely manner. I recommend them any time a professor or student inquires about next-gen sequencing.”

    Researcher

    Texas Tech University

  • “In addition to providing high quality results, the staff at Admera Health supplied detailed and rapid feedback and assistance in all regards. [The team] were incredibly helpful and gave timeous responses.”

    Lecturer

    University Of The Witwatersrand, Johannesburg

  • “Fantastic customer service, highly responsive, fast data delivery, and highest quality data. Everything worked great.”

    Assistant Professor

    Baylor College of Medicine

  • “As always, very satisfied with Admera's service. From quote to data in less than two weeks, and that is including a technical hiccup that they solved in stride. Will use them again and again.”

    Assistant Professor

    Rutgers University

  • “We gave you two incorrect barcodes, but the staff at Admera found the two unlisted barcodes and sent them to us without us needing to ask. We really appreciate the care taken with our data.”

    Assistant Professor

    Rutgers University

  • “We work with aDNA and other degraded samples and appreciate the (1) quality of our data given the sample degradation and (2) the incredibly fast speed of service. We stopped using our last sequencing company after they completely stopped responding and returned data 3 months late so this is beyond anything we expected.”

    Researcher

    Arizona State University