Map the genetic landscape before your clinical trial
Atlas qDMS delivers high-resolution data for every resistance mutation: dose-aware intelligence to design smarter trials and de-risk your pipeline.
90% of drug candidates fail after entering clinical studies
~50% of these failures are due to preventable efficacy gaps. Atlas qDMS is engineered to identify these liabilities in the lab (where they cost pennies) rather than in the clinic, where they cost programs.
We’re making it possible to predict drug efficacy early and accurately.
Atlas Biotech brings clarity to discovery by characterizing target liabilities, profiling safety windows, and engineering Custom Models to ensure biological relevance, so you can build pipelines with confidence and bring breakthrough therapies to market faster.
QDMS: Our Breakthrough Method
With state-of-the-art quantitative deep mutational scanning (qDMS), Atlas Biotech can reveal which mutations respond to or resist your drug by testing thousands of variants at once. Unlike traditional DMS, we directly measure dose-response in patient-relevant conditions, leveraging translational pharmacology for precise predictions.
Secure the Whole Program
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Cell Line Generation
BIOLOGICALLY TRUE DATA
Standard cell lines often yield standard failures. We engineer custom, patient-relevant cell models (Custom Lines) so your qDMS efficacy data reflects biological reality, not just a lab artifact. -

Specificity Screenings
THE SAFEGUARD
Efficacy means nothing if toxicity kills the program. While qDMS confirms the hit, our Specificity Screening (TELTALE) confirms the safety, predicting adverse events before they reach the clinic. -

Functional Genomics
DURABLE THERAPIES
Pairing qDMS resistance maps with our Functional Genomics (Bypass) screens reveals how tumors rewire to survive: helping you design durable therapies that result in successful clinical trials.
Our Partners
We can define your timeline and library strategy in a single 30-minute technical review.


