EXCITING NEWS!
We’ve Acquired BioEcho Life Sciences! Explore Innovative Nucleic Acid Extraction Solutions:
Transcriptomics
Understand gene expression in different cell populations
NGS RNA-seq Services
smRNA-seq
miRNA-seq
Short non-coding RNAs like small RNA (smRNA) and microRNA (miRNA) regulate expression post-transcriptionally and their roles are critical in further understanding gene expression.
Scalable high throughput capability on Illumina platforms
Quick turnaround
QIAgen, NEB, Illumina, Takara, and other platforms
scRNA-seq
Admera offers bulk RNAseq at ultra-low input levels, near single cell level. Contact us for more information.
mRNA-seq
Analyze gene expression, presence of novel isoforms, alternatively spliced transcripts, gene fusion events, etc.
Flexible sample type, including FFPE, blood, cell pellet, etc.
Scalable high throughput capability on Illumina platforms
Bioinformatic Support including QC, Alignment, Gene feature counting, DE analysis, GO/KEGG analysis, Alternative splicing, and more
Total RNA-seq
Quanitification of non-coding RNA carries valuable information about cellular functions.
Technical and bioinformatic support to strategize for specific study
Review non-coding RNAs such lncRNA, tRNA transfer RNA, scRNA, snRNA, snoRNA, lincRNAs and others
Flexible sample types including fresh frozen tissue, cell pellet, FFPE
Metatranscriptomics
Join the growing understanding of how the microbiome influences health with metatranscriptomics analysis.
Extraction from variety of sample types include environmental samples
Industry leading turnaround time
Flexible sample input
Shotgun sequencing
High-Throughput RNA-seq
DRUG-seq
Digital RNA pertUrbation of Genes (DRUG-seq) produces Illumina-compatible 3’ mRNA-seq libraries from cell lysates in 96-, 384-, & 1536-well format for mechanistic studies in a one-day workflow.
Unbiased, massively parallel, whole transcriptome profiling
RNA extraction-free library preparation with direct reverse transcription from cell lysate, skipping RNA isolation procedures
DRUG-seq captures transcriptional changes from known & novel compounds and can detect differences between compound treatment & CRISPR perturbation on the same target
BRB-seq
Bulk RNA Barcoding and Sequencing (BRB-seq) generates Illumina-compatible 3’ mRNA-seq libraries from total RNA in 96- & 384-well format, with just 2 hours of hands-on time.
Accurate bulk RNA-seq method with comparable performance to standard RNA-seq approaches (e.g. TruSeq)
Lower library preparation cost & time equates to the analysis of more samples or replicates
Replace large RT-qPCR assays to measure transcriptome-wide gene expression
Advantages of Working with Admera Health
Quick Turnaround Time
Our team operates with urgency to deliver results while maintaining industry leading data quality.
US-Based Operations
Your sample processing is efficient and secure with us. We perform all NGS solutions in South Plainfield, New Jersey.
Flexible Sample Types
Admera has optimized workflows to support ultra-low input with challenging samples.
