Uncover the right target—and prove it.
We combine single-cell, spatial, proteomics, and bulk datasets into integrated pipelines that:
Estimate and segment target populations
Identify causal genes, pathways, and mechanisms
Pinpoint the causal cell types driving disease
Match targets to the modality most likely to succeed (biologics, small molecules, cell therapy, and more)
Deliver IND-ready data packages, backed by robust, reproducible analysis
All powered by the same domain-specific infrastructure behind our biomarker, QC, and spatial integration pipelines ready to be used in clinical programs and FDA submissions.
Integrated single-cell, spatial, bulk, and proteomic pipelines that surface predictive biomarkers, PD signatures, and TME stratification—including CAR-T biomarker frameworks used in FDA submissions.
Automated, reproducible pipelines for:
Cell-composition analysis
In-process control analytics
Release-criteria development
Multimodal QC data integration
Supporting clinical manufacturing consistency and regulatory requirements.
Pipelines combining spatial data, histology, imaging features, and downstream single-cell integration—enabling biodistribution analysis, tissue-engineering validation, immune infiltration profiling, and mechanism-of-action discovery.
We unify scRNA-seq, ATAC-seq, TCR/BCR, proteomics, and spatial datasets across donors and timepoints to model cell states, clonotypes, and therapeutic responses.
We modernize or rebuild existing pipelines and integrate them with legacy datasets, ensuring reproducibility, scalability, and downstream compatibility.
Our own batch-resistant, pan-organ classification platform, MiraTyper, standardizes cell-type definitions across studies—eliminating the “every dataset, new labels” problem.
Lean on our experience in building and leading analytics teams, from startups to big pharma. We can advise on strategy, partnership opportunity evaluation, and technology and process.
Business analytics strategy:
Are you an investor and thinking about investing in a promising biotech with a complicated drug discovery analytics platform?
We will provide a 30 min free, complimentary consult that would help determine if our skill sets meet your goals. The call will be completely confidential, but NDA free. This call would be limited to general advice and will not provide any specific solutions.
We can consult on specific questions regarding your project. Potential discounts are available for small clients and startups. We understand how hard it is to get started. Per/hr basis.
We can handle all the data from design of experiments, to data transfer, and report generation. We have state of the art pharma grade security and best practices for handling data in a completely confidential manner. Pricing dependent on scope.