Industries · Cell & Gene Therapy

Cell & Gene Therapy

OMICS4 runs the molecular characterization behind your cell engineering and gene therapy programs (transcriptomic profiling, vector and expression quantification, and QC), bookable in-house and through our partner network.

Overview

Molecular characterization at every stage

Engineering a cell or gene therapy product demands tight molecular characterization at every stage. OMICS4 supports these programs with transcriptomic profiling and vector expression analysis run in-house, with specialist vector and cell-therapy expertise from our partner CTI Biotech available where a project calls for it.

Partner spotlight: CTI Biotech For programs that need specialist vector engineering or cell-therapy process support beyond our in-house platforms, we work with CTI Biotech under the same single point of contact and QC framework as our own lab.

OMICS4 capabilities

Built for CGT process development

Transcriptomic characterization of engineered cells

Bulk RNA-seq framing before/after transduction or gene editing.

  • Pre/post-modification transcriptional comparison
  • On- and off-target signature screening
  • Batch-to-batch consistency profiling across lots
See related platform

Vector integration & expression profiling

Molecular readouts on vector behavior across development stages.

  • Integration site mapping support
  • Vector copy number & expression quantification (qPCR/ddPCR)
  • Transgene expression kinetics across passages
See related platform

Molecular QC support across development stages

QC scoped to your process development and release milestones.

  • Identity & purity QC from PD to release
  • Contamination and mycoplasma screening handoff
  • QC criteria aligned to your CMC milestones
See related platform

Vector-aware bioinformatics, via GenXMap

Custom pipelines built per construct, not a generic template, delivered by GenXMap's Computational Biology & AI layer on top of our wet-lab data.

  • Reproducible, containerized pipelines per program
  • Vector-aware alignment & quantification
  • Audit-ready reporting for regulatory files
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

Your process runs under GMP-adjacent process development, with strict batch and lot traceability.

How OMICS4 adapts

Every sample is tracked with your internal lot IDs end-to-end; reports are structured to slot directly into your batch records.

Their reality

Vector and cell line constructs vary program to program, so off-the-shelf pipelines don't fit.

How OMICS4 adapts

Pipelines are reconfigured per construct (vector backbone, promoter, edit site) rather than run through a generic RNA-seq template.

Their reality

Development timelines are milestone-driven: IND-enabling studies, potency assay lock, tech transfer.

How OMICS4 adapts

Turnaround and QC checkpoints are scheduled against your milestone calendar, not a fixed lab queue.

Their reality

Data needs to feed into your existing ELN/LIMS and regulatory documentation.

How OMICS4 adapts

Deliverables are exported in the format your team already uses: CSV/Excel for LIMS import, PDF summaries for regulatory binders.

Have a project in this space?

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

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