Sequencing & Transcriptomics (Targeted/Full NGS + RNA-seq)

Link Genotype and Expression to Functional Response

A sequencing and transcriptomics add-on, including targeted NGS, whole-exome, whole-genome, and bulk or single-cell RNA-seq, integrated with ex vivo drug-response data.

From description to prediction

Sequencing alone describes biology; paired with functional response, it predicts it. We connect mutational and expression profiles to measured ex vivo drug sensitivity to surface candidate biomarkers and mechanisms.

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What the add-on covers

DNA sequencing

Targeted NGS panels, whole-exome (WES), and whole-genome (WGS) — with mutation summary, gene list, variant allele frequency, and predicted impact.

Transcriptomics

Bulk RNA-seq andsingle-cell RNA-seq with pathway analysis, cluster identification, and UMAPvisualization.

Integration

Genotype and expression correlated with drug response to generate predictive-biomarker and enrichment hypotheses.

How it attaches

Pairs with any live-cell service and the natural companion to Biomarker Validation and Drug-Resistance Profiling.

Key Deliverables

01
Targeted NGS/WES/WGS with mutation summary, VAF, and predicted impact
02
Bulk and single-cell RNA-seq with pathway, clusters, and UMAP
03
Genotype/expression-to-response correlation for biomarker discovery
04
Integrated multi-omic report with fast turnaround
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Let's Talk

Add SEquencing to your Study

A scientist — not a sales desk — will scope a tailored study and return a design and timeline.