new cancer cases worldwide in 2022
With about 9.7 million deaths. IARC projects more than 35 million new cases a year by 2050.19
WhySquared works where artificial intelligence meets molecular biology and cancer research. We help labs and teams turn sequencing data, protein models and clinical evidence into decisions they can defend.
Cancer cases are rising faster than our capacity to study them, and most drug candidates still fail late, after years of work. AI won't fix that alone, but it changes where the time and money go.
With about 9.7 million deaths. IARC projects more than 35 million new cases a year by 2050.19
Lack of efficacy and toxicity explain most failures, the bulk of the cost lands at the end of the process.20
At a cost of around US$1 billion per successful drug. Shortening the early, computational stages is where AI is already proving useful.20
Five stages where models are already changing molecular biology and oncology, what each is used for, and the published result behind it.
Most of the progress on this page comes from four families of AI. Knowing which one fits a question is half the work.
Trained to fill in missing letters across billions of DNA or protein sequences. To do that well, they learn which patterns are conserved, which tells you which changes are likely to matter.
Learns how a chain of amino acids folds into a 3D shape, and how that shape fits against DNA, RNA or a drug, from structures scientists have already solved.
Starts from noise and refines it, step by step, into a new protein, antibody or binder that meets a target. The same idea behind image generators, applied to molecules.
A language model that plans, uses tools, reads the results and decides what to do next, working for hours across databases, code and, increasingly, lab equipment.
In twelve months Anthropic went from connecting Claude to lab software to running its own wet lab. The most talked-about result so far: an enzyme system in bacteriophage DNA that Claude's agents flagged, with the caveat that nobody yet knows what it does.
Connectors for Benchling, BioRender, PubMed, 10x Genomics and Synapse.org, plus a skill for single-cell RNA-seq quality control. Customers named include Sanofi, Broad Institute and Novo Nordisk.3
Anthropic acquires the stealth AI-biotech startup in a deal reported at around US$400 million.6
A research product built for reproducibility, which in a demonstration identified drug candidates for phenylketonuria. Anthropic also starts a small number of preclinical programmes for diseases drugmakers tend to neglect.4,7
A Bay Area lab where Claude controls equipment through the Model Hardware Standard, co-developed with HHMI. In an evaluation, Claude Mythos 5.1 produced 12 high-affinity binder candidates with a reported 50% hit rate, against a typical 10–15%.5
Agents screened public sequence data and flagged an enzyme system, mainly in phages, with a CRISPR-like repeat array. Human researchers did the lab work. Pre-print on bioRxiv.1,2
Peer-reviewed papers, trials and major announcements from the last two years. Every figure links to its source.
Google DeepMind's model takes up to a million base pairs and predicts 5,930 human genetic signals at once, from gene expression to splicing.
Arc Institute's fully open model, trained on 128,000+ genomes, can flag disease-causing mutations and design genome-length sequences.
Structures of proteins together with DNA, RNA, ligands and ions, available free to researchers through AlphaFold Server.
David Baker for computational protein design; Demis Hassabis and John Jumper for AlphaFold's structure prediction.
EvolutionaryScale's model generated esmGFP, a glowing protein its authors compare to 500 million years of evolution.
Across 52 targets with no known antibody binders, testing up to 20 designs each, it found binders for half of them in one round.
The first randomised trial, with over 100,000 women in Sweden, found fewer cancers missed between screens.
142,250 people in England. The primary endpoint was not met, but stage IV diagnoses fell in a secondary analysis.
Biohub, the US Department of Energy, NIH, Google DeepMind, Isomorphic Labs and Meta commit to open, AI-ready biological data.
A government-funded UK trial testing AI on routine mammograms across 30 sites, backed by £11 million through NIHR.
On Protocol QA, a benchmark of questions about experimental protocols, Claude Sonnet 4.5 edged past the human baseline of 0.79.
The AlphaFold spin-out says its first AI-designed drugs should enter clinical trials by the end of 2026, a year later than first planned.
A quick map of the systems on this page by the kind of data they work with. Filter by modality to see your options.
WhySquared sits between the research and the lab bench: choosing the right model, wiring it into real data, and checking the output the way a diagnostics lab would.
Pipelines that combine genome models such as AlphaGenome or Evo 2 with curated databases, so variant calls arrive with evidence attached rather than a bare score.
AlphaFold 3 and design models used to shortlist targets and binders before anything is ordered, with clear criteria for what goes to the bench.
Quality control, clustering and annotation for single-cell RNA-seq and bulk data, delivered as reproducible notebooks your team can rerun.
Agents that search PubMed and pre-prints, extract findings into structured tables and keep every claim traceable to a paragraph in a paper.
Model evaluation designed with ISO 15189 and GLP habits: defined acceptance criteria, held-out data, error analysis and documentation an auditor can follow.
Getting instrument output, LIMS and electronic notebooks into a shape models can use, and connecting tools like Benchling to AI assistants safely.
Every engagement follows the same five steps, so you can stop after any of them with something useful in hand.
Pin down the scientific question and the decision the answer has to support.
→ one-page briefCheck what data exists, its quality, consent and licensing, and what's missing.
→ data readiness reportBenchmark candidate models on your own data against a simple baseline.
→ comparison and recommendationTest against acceptance criteria agreed up front, on data the model hasn't seen.
→ validation reportCode, documentation and training so your team can run and question it.
→ working pipelineBiology AI raises real questions about safety, privacy and over-reliance. These are the rules we work to.
We follow the field's lead on dual-use risk: Evo 2's developers, for example, left human-infecting pathogens out of its base training data. We don't take on work aimed at making pathogens more capable.9
Work involving health data follows UK GDPR, uses the minimum data needed and runs inside your own environment wherever possible.
No model output feeds a clinical or experimental decision without review by someone qualified to judge it.
Model versions, parameters, code and data snapshots are recorded, so any result can be rerun and checked later.
Good results come with fine print. We read it before we recommend anything, and we think you should see it too.
ART's role in phages is still unknown, and only the first experiment, showing the array is expressed as short RNAs, has been reported.1
NHS-Galleri did not show a significant drop in combined stage III–IV cancers. The stage IV reduction is a secondary finding awaiting peer review.16
Isomorphic Labs expected AI-designed drugs in trials by the end of 2025. Its CEO now says the first trials should come by the end of 2026.18
Even in Anthropic's most autonomous work, scientists chose the question, reviewed candidates and did every experiment by hand.1
WhySquared is led by Yılmazer Yılmaz, a molecular biologist with experience in high-throughput clinical diagnostics and hands-on lab research. The view from the bench shapes how we judge AI: a prediction is only useful if a lab can act on it and an auditor can trace it.
Often not. Many of the strongest models are pre-trained on public data, so a smaller, well-curated set of your own data is enough to test whether they help. Part of the data audit is telling you honestly if what you have is sufficient.
It depends on the model. Licences vary widely: AlphaFold 3's code and weights, for example, were released for academic use, and AlphaFold Server is intended for non-commercial research. We check the terms for every model before recommending it.10
No. It changes what reaches the bench. Even in Anthropic's ART discovery, every experiment was done by human researchers. The realistic gain is testing fewer, better candidates.1
We agree the data handling up front, keep processing inside your environment where possible, and use only what the question needs. Nothing is sent to an external AI service without your explicit approval.
Usually the first two or three steps of our process: a scoping brief, a data audit and a small pilot comparing models on your data. It's designed to give you a clear go or no-go before any larger commitment.
Primary announcements, journals and trial reports used on this page. Figures reflect what each source reported at the time of writing.
Tell us what you're working on, the data you have and the decision it needs to support. You'll get a short, honest assessment of whether AI can help, and how we'd check that it does.
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