Industries · Drug Discovery & Biotechnology
Translational biomarker pipelines to accelerate discovery programs.
A compound that works is not the same as a compound you can explain. Mechanism of action, the targets that actually move, and whether a readout will translate are analysis questions, and they decide go or no-go long before the next study is designed.
For the stage gate where the intended target is no longer enough: it establishes what the compound actually does to the cell, which targets move on their own, and which move only downstream.
We are not a service provider taking an order and running a protocol. The design is ours: which off-target movements are signal and which are downstream consequence — a call that requires knowing the pathway, not just running the differential expression. That is what an R&D team working on the subject brings, and it is the difference between buying an analysis and running a programme.
Dose and time series analysed as series, not as a set of isolated comparisons.
Ranking what moved, and separating cause from downstream consequence.
Hit calling with the error rate stated, so a shortlist can be acted on.
Candidates carried from model to cohort with the same definitions throughout.
Versions, parameters and thresholds recorded per study, ready for an internal review.
Analysis plans are scoped per stage gate, so results land in time for a go or no-go rather than after it.
Coded sample identifiers and NDA-governed workflows keep target and compound identity compartmentalized, and outputs are formatted to integrate with the informatics stack you already run rather than replace it.
Methods with exact tool versions, parameters and thresholds. QC and cohort-level figures. Statistical results. An interpretation written against the biological question you started from.
Built to be audited or reproduced by a third party.
The laboratory work behind these analyses runs on OMICS4, GenXMap’s platform site. Sample requirements, shipping and turnaround are published there.
We also take on data we did not generate. An existing dataset, from an earlier study or from another provider, is analysed on its own terms. What decides the work is the question and the metadata that comes with it, not who ran the sequencer.
Book the platforms on OMICS4Case studies for this industry are in preparation: get in touch to discuss a project directly.
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