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

Non-coding 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

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

Other NGS Services That May Be of Interest

Bioinformatics

Single-Cell Sequencing

Epigenomics