Understanding the positional effects of potential integration sites is therefore critical both in designing effective and safe cell therapies as well as in designing biologics manufacturing systems.
Annogen’s Integration Mapping (AIM™) technology barcodes >100,000 genomic loci to determine the most optimal sites for expression of a transgene.
We start by defining what the design or integration site needs to support: expression strength, stability, cell-state response and the level of control required for the therapy.
AIM™ integrates a barcoded reporter or therapeutic construct across more than 100,000 genomic loci, making each integration site individually traceable.
Barcode-linked NGS/RNA readouts show how genomic position influences expression behavior, including strength, stability, variability and condition-specific response.
The result is a ranked view of candidate integration sites, based on how well they support the intended therapeutic expression profile.
AIM projects can be completed within as little as 3 months.
A broader view of where your construct can work.
When your therapy allows targeted integration, the genomic locus becomes part of the design. Known safe-harbor sites can be useful, but may not provide the expression behavior your construct requires.
AIM™ expands that decision space by comparing transcriptional activity across more than 100,000 genomic integration sites, revealing which genomic environments support stable, controlled therapeutic expression.
This moves integration-site selection from assumption to experimental evidence.


















Explore how tailored gene expression systems support safer, more controlled cell and gene therapies.
Engineer promoters and enhancers when regulatory sequence design drives therapeutic expression control.
Our focus is the design and validation of gene regulatory elements, including promoters and UTRs. We do not develop cell lines or run production ourselves, though we work alongside the partners who do.
We have run the platform in CHO-S in-house and cast a wide net across sequences to minimise the chance of missing strong elements. We can discuss validation in the specific CHO lineage you use.
Alongside regulatory-element design, we can screen for genomic sites that support stable, high expression, which matters for lentiviral and retroviral integration and for stable cell lines. It uses the same barcoding principle as our promoter work.
Robustness comes from scale and controls: each element or expression locus is represented by many barcodes, we include reference and negative controls, and we use biological replicates and defined specificity thresholds to separate real signal from noise. We are glad to share the statistical approach with your team.
We imagine there could be some question you want to ask us. Discover the most frequently asked questions about this subject right here.
Let’s start with your dreams.
Share your challenge, question or ambitions. We will help you explore how our off-the-shelf promoters can support the decisions ahead.
We use cookies to personalize content, provide social media features, and analyze our traffic. We also share information about your use of our site with our analytics partners. You can change your preferences at any time. For more information, please see our Privacy Policy and Cookie Policy.