CRISPR Intelligence: Advanced Therapeutic R&D Platform
An advanced R&D platform for designing, predicting, and validating CRISPR-based therapeutics with unparalleled precision and speed.
CRISPR Intelligence: Advanced Therapeutic R&D Platform
In-silico means "in silicon" - referring to computer-based analysis that simulates and predicts biological processes.
An advanced R&D platform for designing, predicting, and validating CRISPR-based therapeutics with unparalleled precision and speed.
Core Capabilities
3 advanced AI-powered capabilities designed to transform your workflow
Predict: CRISPR Target Validation
Capability Deep Dive
Technical Approach
ClinVar validation for variant impact prediction. Analyzes target sites for functional variants that could affect gRNA binding efficiency.
The Value Proposition Flywheel
Strategic advantages that create a self-sustaining cycle of value delivery for each target audience.
For Scientists & Research Labs
- Design with Unprecedented Confidence: Leverage best-in-class AI to design highly potent and specific guide RNAs from the start, dramatically increasing the success rate of your editing experiments and minimizing costly validation cycles.
- Go from Raw Data to Actionable Insight, Faster: Let our AI Co-Pilot handle the heavy lifting of complex NGS data analysis and therapeutic contextualization, transforming your experimental results into clear, decision-ready insights in a fraction of the time.
- Democratize Advanced Computational Biology: Access a suite of sophisticated AI tools for variant effect prediction, off-target analysis, and experimental design, without needing a dedicated bioinformatics team. Focus on your science, not on building analysis pipelines.
- Produce High-Impact, Publishable Results: Generate higher quality, more reproducible data with AI-guided experimental design and analysis, strengthening your publications, grant applications, and contributions to the field.
For Biotechnology & Pharmaceutical Leaders
- De-Risk Your Therapeutic Pipeline: Make more informed go/no-go decisions with AI-driven insights into target validity, off-target safety, and potential translational hurdles, significantly reducing the risk profile of your preclinical programs.
- Accelerate Timelines to the Clinic: Shorten the entire discovery and preclinical development cycle for CRISPR therapies by streamlining design, automating complex analysis, and contextualizing results for therapeutic viability from day one.
- Build a Moat Around Your IP: Strengthen your intellectual property position with novel, highly optimized, and well-characterized gene editing strategies and therapeutic candidates designed and validated through the platform.
- Maximize Your R&D Investment: Improve the overall efficiency and success rate of your therapeutic programs, ensuring your resources are focused on the most promising candidates and strategies, leading to a higher potential return on investment.
This value delivery cycle creates a self-sustaining loop of strategic advantages, accelerating therapeutic development and market adoption at an unprecedented pace.
Our platform operationalizes these capabilities into a structured, seven-step in-silico workflow that delivers real business value:
From data curation to final validation, our automated pipeline transforms complex biological challenges into engineered therapeutic solutions.
1. Problem Framing & Data Curation
Assemble genomic loci, clinical variants, and DMS datasets to define the therapeutic target space.
2. Target Assessment (Discriminative)
CrisPRO zero-shot ΔLL scoring in 8,192 bp context to evaluate on-target activity.
3. Mechanistic Triage & Hypothesis
CrisPRO embeddings for exon/intron classification to understand the biological impact.
4. Design (Generative)
CrisPRO proposals with Enformer+Borzoi scoring to generate high-efficacy gRNA candidates.
5. In-Silico Validation
Aggregate scores with structure metrics (pLDDT/PAE) to validate designs computationally.
6. Feedback & Calibration
Lightweight supervised heads on CrisPRO embeddings to continuously refine and calibrate models.
7. Reporting & Provenance
Evidence reports with traceable citations and complete data provenance for regulatory and research needs.
Strategic Conclusion
Explore Other Co-Pilots
Chemo Co‑Pilot: In‑Silico Chemotherapy Guidance
In‑silico chemotherapy insight: see which drug classes may fit a patient's genetics—before you treat. Clear signals, confidence, and sources (research‑mode).
Clinical Trials Co‑Pilot: In‑Silico Trial Matching
Find matching trials in minutes. Clear eligibility and a shareable one‑pager (research‑mode).
Pathway View: What's Driving This?
A simple biology story for each case: which pathways look most involved, and how that ties to therapy (research‑mode).
Therapy Fit: In‑Silico Drug Ranking
See which drug classes may fit a patient's genetics—before treatment. Clear ranking, confidence, and sources (research‑mode).
Toxicity Risk (Germline): In‑Silico Side‑Effect Hints
See simple, genetics‑aware side‑effect hints to plan conservatively—before treatment (research‑mode).