Book an Analysis Session
Configure your session parameters. Our Lead Expert will review this context to prepare your computational environment before we meet.
We provide the Automated Validation and Technical Due Diligence required to turn your discovery into a Defensible Asset. Whether you are validating a target or preparing for acquisition, we ensure your science survives scrutiny.
Data Vault Ingestion
Secure connection established. Metadata harmonized.
Cohort Matching
Signal replicated in 4 independent datasets.
Patient Subgroups
Predictive accuracy > 0.8 in 6 conditions.
Glass-Box Export
SUCCESSFUL
Pharma spends billions buying assets that disintegrate upon validation. Why? Because the science lacks global context and the analysis lacks technical rigor.
If your data cannot survive an external audit or replicate in independent cohorts, you do not have an asset. You have a liability.
Looking at your dataset in isolation is blinding. Without benchmarking against global data, you are flying without a map.
50% of preclinical research fails to replicate. Investors know this. They will check. Will you pass?
Standard analysis is a liability. In an industry where 50% of published research fails to replicate, a pipeline that cannot withstand due diligence makes your asset worthless.
We don't just process data; we engineer permanence. We act as the System of Record for your biological intelligence, generating a "Glass Box" audit trail that guarantees your results are reproducible—bit for bit—five years from today.
Benchmarking against raw public data is futile. We validate your findings against our Harmonized Global Atlas, filtering out technical artifacts to reveal true clinical signal.
Immutable by design. We freeze every parameter, container, and version. When investors demand technical due diligence, you don't offer explanations—you deliver a verifiable audit log.
We combine aggressive scientific expansion with defensive technical auditing.
We benchmark your findings against our Curated Bio-Atlas of 12,400+ Harmonized Cohorts. We identify where your target works, who it works for, and prove its robustness beyond your lab.
Great science is worthless if the code breaks during an audit. We act as your Data Vault, freezing your analysis in time to guarantee pixel-perfect reproducibility five years from now.
We have decoupled execution from interpretation. By replacing high-variance manual analysis with deterministic computational engines, we focus our scientific resources exclusively on high-value strategic validation.
A multidisciplinary team of domain experts defines the biological strategy and validates automated findings.
Automated pipelines handle normalization, QC, and statistical testing at scale. Zero human error. Infinite scalability.
We do not provide static reports. We provide a Regulatory-Grade Audit Trail. This is a secure, immutable record of every computational step, benchmark, and validation metric—ready for immediate technical due diligence.
>> Received packet: raw_reads_v2.fastq.gz (145 GB)
>> Calculating Checksum...
>> SHA-256: e3b0c44298fc1c149afbf4c8996fb92427ae41e4649b934ca495991b7852b855
>> Signature Verified. Data Locked in Vault.
>> Analyzing Target: CTLA4
>> Artifact Detection: DETECTED (Batch Effect in Cohort B)
>> Auto-Correction: APPLIED (Combat-Seq)
Global Atlas Benchmarking (n=12,400)
>> PASS: Signal exceeds noise threshold in 94% of reference cohorts.
>> Generating Compliance Report...
>> Review Board: DSB-04 (Lead)
>> Status: DUE_DILIGENCE_READY
Tailored Intelligence For Every Stage
Don't rely on pitch decks. Run a "Technical Audit" on prospective portfolio companies before you wire the funds. Verify the asset exists and replicates.
FOR DEAL FLOW →Prepare for the exit from Day 1. We act as your external Due Diligence partner, ensuring your data integrity stands up to investor scrutiny during Series A/B.
FOR EXIT STRATEGY →Automate your Data Management & Sharing Plans. We provide the "System of Record" infrastructure for TTOs and Core Facilities.
FOR GRANT COMPLIANCE →DEFENSIBLE ASSETS
Your biological data is fragmented. We unify it. A secure, immutable cloud vault that becomes your organization's single source of truth.
Built on 21 CFR Part 11 principles. Automated generation of immutable figures and audit trails that survive technical due diligence.
Don't benchmark against noise. We provide access to our curated atlas of harmonized public data, cleaned for clinical relevance.
We don't sell hours. We sell uptime. Our automated pipelines process terabytes of data overnight, standardized and error-free.
ARCHITECTURE: CONTINUOUS_VALIDATION_PIPELINE
Raw FASTQ/BAM files are ingested via secure API. Data is immediately encapsulated in a Dockerized Environment to neutralize version dependency issues.
Automated QC scripts run aggressive "Unit Tests" on your samples. We detect batch effects, low reads, and outliers before compute resources are wasted.
Your clean data is projected onto our Global Reference Atlas. We measure signal robustness across 12,000+ external cohorts instantly.
Pipeline execution is halted. Containers, parameters, and results are hashed (SHA-256). A "Frozen State" is written to WORM (Write Once, Read Many) storage.
The system generates the "Glass Box" artifact: a self-contained, executable package containing your validation proof, ready for Due Diligence.
We are currently onboarding partners for Q4. Secure your data vault today and establish the audit trail that protects your valuation.
Configure your session parameters. Our Lead Expert will review this context to prepare your computational environment before we meet.