Industries · Immuno-oncology

Immuno-oncology

OMICS4 runs the multi-omics profiling behind your tumor microenvironment studies (bulk and single-cell RNA-seq, immune profiling and biomarker sample workflows) via our in-house platforms.

Overview

Tumor microenvironment, characterized

OMICS4 characterizes the tumor microenvironment through integrated multi-omics, helping translational teams generate the biomarker data linked to immune response and treatment outcome, run end-to-end via our in-house platforms.

OMICS4 capabilities

Built for translational oncology

Tumor microenvironment multi-omics profiling

Tumor and immune compartments characterized at multiple layers.

  • Bulk and single-cell RNA-seq of tumor & immune compartments
  • Spatial context when tissue architecture matters
  • Multi-omics layering across available sample types
See related platform

Immune cell composition profiling from bulk & single-cell data

Sample-level sequencing that feeds cell-type composition and subtype analysis.

  • Cell-type composition estimation from bulk RNA-seq
  • Single-cell library prep & sequencing for immune subtyping
  • Batch-controlled processing across cohorts
See related platform

Biomarker discovery & validation for checkpoint response

Responder signatures validated across independent cohorts.

  • Responder vs non-responder signature discovery support
  • Orthogonal biomarker validation (qPCR/ddPCR)
  • Biomarker packages structured for translational review
See related platform

AI-driven interpretation of immune signatures, via GenXMap

ML models and dashboards linking signatures to outcome, delivered by GenXMap's Computational Biology & AI layer on top of our wet-lab data.

  • ML models linking immune signatures to outcome
  • Interactive dashboards for cohort-level exploration
  • Reproducible, versioned models per study
Talk to our team
Case studies Case studies for this industry are in preparation, so get in touch to discuss a project directly.

How OMICS4 adapts

How OMICS4 adapts to your process

No two programs run the same workflow. Here is how OMICS4 fits into what you already have in place.

Their reality

Samples are often scarce, heterogeneous biopsies collected across multiple clinical sites.

How OMICS4 adapts

Protocols are built for low-input, FFPE-compatible, multi-site sample sets with harmonized QC.

Their reality

Cohorts evolve over time as trials enroll: data needs to accumulate, not restart.

How OMICS4 adapts

Processing is versioned so new patient batches are integrated into the existing cohort, not reprocessed from scratch.

Their reality

Translational teams need results that connect back to clinical outcome and treatment arms.

How OMICS4 adapts

Molecular findings are reported alongside your clinical/treatment metadata, not as a standalone omics dataset.

Their reality

Regulatory and IRB constraints shape what data can move where.

How OMICS4 adapts

Data handling is scoped to your consent and IRB framework from the outset.

Have a project in this space?

Let's talk about your sample, your question, your timeline.

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