Scienvera is a small research-engineering studio. We build our own AI researcher, a tool that cites every claim against the literature, and we turn scientists' algorithms into real applications: desktop with Tauri and Qt, web and backend with Spring, deployed on cloud.
Evidence is mixed but trends positive: three cohort studies report reduced recurrence; one RCT shows no significant effect.
We built it for ourselves first. Proof of how we work. It began as a citation finder and claim-checker; every query runs against the academic record, so what you get back is traceable, not plausible-sounding.
Ask in plain language. Every sentence links to the paper it came from. No source, no claim.
Paste a statement. Scienvera cross-references PubMed and returns supported, unverified, or contradicted, with evidence on both sides.
Filter by venue, year, and study type. Surface the primary sources behind a topic in seconds, ranked by relevance.
Deep-learning research in computational oncology: multi-omic integration and cancer subtyping, evaluated on real patient cohorts.
A Transformer autoencoder integrates RNA-seq and 450k DNA-methylation data into a shared latent space. Unsupervised clustering of that space splits 250 patients into two risk groups with significantly different overall survival, a prognostic signal single-omic analysis misses. The separation holds across 100 bootstrap runs (mean ARI 0.92) and stays significant in multivariable Cox regression (HR 1.99, adjusting for age, sex, and histology).


A gated cross-attention mechanism fuses gene-expression and mutation features: each modality attends to the other while a learned gate controls how much each contributes. On a held-out test set of 267 patients it classifies the intrinsic molecular subtypes (Luminal A/B, HER2-enriched, Basal) at 92.8% accuracy, and the learned fusion layer separates the subtypes cleanly in t-SNE.
We publish our methods and release code. Links resolve as preprints and repositories go live.
Most research algorithms never leave the notebook. We take a method or model and turn it into an application a lab or clinic can actually use, the same way we built our own.
Give us a method or model; we deliver a tool your users can run. Desktop and clinical apps with Tauri and Qt, web and backend with Spring.
Deep-learning models for genomics and multi-omic data: stratification, subtyping, and integration, from prototype to validation.
Citation-grounded answer systems, claim verification, and retrieval over scientific corpora. The engine behind tools.scienvera.
Containerized deployment on Kubernetes, CI/CD, and observability, so models and services ship and stay shipped.

Builds the models and the platform end to end: research, backend, and infrastructure.
The team is closed for now, with no open roles. This is a solo effort while the research and platform take shape.