Admera Health

Thank you Philly BioBreak for this morning’s insightful panel on “Biotech Funding Insights: Strategies for Growth & Success!” Great, engaging conversation with Philadelphia’s fantastic biotech community, cheers! Admera Health

Elevate your research using a multi-omic approach to simultaneously profile the transcriptome & epigenome at the single-cell level. Using the Chromium Single-Cell Multiome ATAC + GEX assay, characterize novel cell types and states, & uncover complex gene regulatory networks to multiply your discovery. Interested in learning more about single-cell multi-omic studies? Connect with our team to get started: https://hubs.ly/Q02QvJ5H0

Study spatial biology with unprecedented field-of-view. Using Stereo-seq technology, we gain spatial insights with subcellular resolution and customizable field-of-view with a chip size that can be expanded up to 13cm x 13cm to accommodate your project's scale.   Learn more about Stereo-seq capabilities with a Certified Service Provider: https://hubs.ly/Q02Q8BCq0

Take advantage of new RNA-Seq pricing and promotions at Admera Health. We’re pleased to introduce new pricing for our comprehensive mRNA-Seq service. Maximize your savings and get your first RNA-Seq data analysis project free of charge. Inquire with a team member to align your next project: https://hubs.ly/Q02P88qy0

Poor-quality FFPE samples present both challenges and opportunities for any researcher. While FFPE processing is a practical method for storing samples long-term, the fixation process results in chemical modifications to cellular DNA, RNA, & proteins, increasing chances of encountering sequencing artifacts downstream. The sheer quantity of FFPE samples worldwide makes these precious resources valuable to prospective and retrospective analysis. With the ability of next-generation sequencing (NGS) to assemble genomic information from millions of short DNA fragments, it has been suggested as the ideal tool for evaluating these highly fragmented tissues. Admera Health is your trusted partner in handling challenging samples. We employ robust extraction, library preparation, and sequencing workflows to ensure you receive quality results to accelerate your research initiatives. Read more about how we can support your FFPE-based research: https://hubs.ly/Q02NGsPb0

Cytosine methylation is an important regulatory mechanism for numerous cellular processes and cancer diagnosis. Revolutionize your methylome analysis with the NEBNext® Enzymatic Methyl-seq (EM-seq™) workflow. EM-seq uses a two-step enzymatic conversion process that is less damaging to the DNA vs. chemical bisulfite methods like whole genome bisulfite sequencing (WGBS). Connect with a team member to get started: https://hubs.ly/Q02N0CKZ0

Our team provides a premium, end-to-end workflow for whole genome sequencing (WGS), enabling the study of an organism's entire genome across a diverse range of sample types. With our comprehensive 1:1 support, we help propel your quest to identify genetic variants involved with health & disease, detect novel biomarkers, or advance conservation & ecology research. Read more about our whole genome sequencing workflow: https://hubs.ly/Q02MLTz30

Single-cell RNA sequencing (scRNA-seq) uncovers the full complexity of cellular heterogeneity, revealing novel insight into new cell types, complex regulatory networks, and key processes involved with cell differentiation and development. Or, compliment your next scRNA-seq dataset to measure chromatin accessibility, immune profiling, or antibody-based protein analysis, even from challenging FFPE samples. Admera Health provides a suite of single-cell solutions to support studies with diverse applications and scales. Visit our website and explore our solutions: https://hubs.ly/Q02MlGL40

Explore complex microbial communities using metatranscriptomics. Metatranscriptomics studies the collective transcriptome from microbial communities to evaluate gene expression community-wide and identify active members within a community and their functions. Metatranscriptomics has been used to study diverse microbiomes found in humans, soils, and aquatic environments. We provide expert support for your research throughout each step of the workflow, from experimental design to data analysis. Let's advance your next microbiome research together with metatranscriptomics: https://hubs.ly/Q02LHTjb0

For a limited time, get your first RNA-seq data analysis project free! Our team of expert bioinformaticians uses advanced pipelines to deliver clear, informative, and interactive results with publication-ready figures. Learn more on our website: https://hubs.ly/Q02LHX1j0