High-Throughput RNA Sequencing Services for Comprehensive Transcriptomic Insights

Generate reliable RNA-Seq data from ultra-low RNA input while preserving precious clinical samples.

Scalable, Customizable End-to-End RNA-Seq Services

Discovery’s Genomics RNA-Seq workflows can be tailored for your specific needs:

Ultra-Low-Input RNA Sequencing Pipeline Validated to Minimize Sample Utilization

Generate high‑quality data using Discovery’s validated ultra–low‑input RNA‑seq workflow, leveraging a proprietary dual nucleic acid extraction method to deliver exceptional precision, accuracy, sensitivity, and specificity from minimal input sample.

Proprietary Dual Nucleic Acid Extraction

Our proprietary extraction method delivers a ~94% success rate which is more than double that of standard off‑the‑shelf approaches. It enables simultaneous DNA and RNA extraction from a single sample, supporting matched sequencing workflows. The process is optimized for even the most challenging sample types, including FFPE tissues and core needle biopsies.

Figure 1. (A) Assessing Discovery’s dual nucleic acid extraction method on FFPE across many indications shows a significant improvement in RNA quality. (B) This enhanced method ultimately resulted in the immediate improvement of RNA-Seq success rate of sequencing with at least 100M PE reads per sample and a mapping rate > 85% by nearly 200%.

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Optimized Methods for Sequencing RNA from FFPE Samples

While FFPE is a gold standard preservation method for immunohistochemistry and other antibody-based analyses, the technique can pose difficulties for researchers wishing to extract nucleic acid-based information, especially gene expression data.

World-Class Bioinformatics and Data Storage Solutions

Comprehensive RNA-Seq analysis includes expression profiling, fusion and splice variant detection, pathway analysis, and flexible data delivery with tiered reporting and storage options.

Your Complete RNA-Seq Solution

From extraction to publication-ready insights, we provide a fully integrated workflow designed for reliability, speed, and scientific excellence.

Sample Prep

Quality That Starts at the Bench

Unlock consistent, high-quality RNA from challenging clinical materials with validated workflows delivering exceptional extraction across blood, FFPE, PBMCs, tissues, and cells.

Proprietary automation ensures RNA quality (DV200 > 30%) in 98% of samples.

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Library Prep

Built for Challenging Inputs

Our validated mRNA-seq and Total RNA-seq workflows enable confident transcriptomics from low-input or degraded samples (25–100 ng, DV200 > 20%).

Strand-specific, scalable prep with rRNA + globin depletion. Fast, automated, and built for large-scale projects.

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Sequencing

Speed Without Compromise

Deliver ultra-fast turnaround without compromising depth or accuracy.

Cross-validated on Illumina NovaSeq 6000 and X Plus, with proven performance across RNA qualities and transcript complexities.

Built for clinical reliability and real-world variability.

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Data Analysis

Insights Delivered Instantly

Through our DNAnexus partnership, sequencing data is delivered at remarkable speed.

Get rapid FASTQ files, secondary outputs (BAMs, VCFs, gene counts), and concierge bioinformatics support for publication-ready data and figures.

Unlock the Potential of RNA-Seq in Clinical Trials

RNA-Seq detects gene fusions and differential expression of disease-causing transcripts, serving as a powerful tool for molecular profiling in clinical trials. Discovery Genomics’ optimized workflows and CAP-accredited, CLIA-certified, and GCLP-compliant laboratory accelerate clinical trial success, aiding in the discovery of potential predictive biomarkers for companion diagnostic development.

RNA-Seq Service Frequently Asked Questions

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