The Story

Why EviGeno exists

The observation

EviGeno was not born from a business idea. It came from a moment I couldn't walk away from. During my career in the healthcare industry, I encountered patients in the final stages of illness who were still searching — not passively waiting, but actively looking for a trial they might qualify for, a therapy approved somewhere else, a molecule no one had told them about. They hadn't given up. They just didn't know where to look.

What I found on the other side of that search was deeply troubling. The patient advocacy industry, for all its good intentions, is structurally limited — it was never built to conduct deep, individualized medical intelligence research tailored to a single patient's molecular profile and clinical history. And when patients and families try to fill that gap themselves, they often encounter something worse: forums full of unverified claims, wellness products masquerading as treatments, and outright fraudulent services targeting people in desperate circumstances. Too many families reach the end of a serious illness having lost both time and resources on interventions that were never grounded in evidence.

The background

My professional foundation spans clinical genomic testing, regulatory submissions, and medical OSINT — work that gave me a precise, working understanding of how molecular profiles translate into treatment options: which mutations are actionable, which biomarkers open or close trial eligibility, and where the interpretive gaps tend to appear in standard NGS reports.

Alongside that, I developed a practiced capability in medical OSINT — open-source intelligence methodology applied to the healthcare domain. OSINT, in its professional sense, is not about searching Google. It is a structured discipline: knowing which sources exist, how to access and cross-reference them, how to validate information across registries and regulatory filings in multiple languages, and how to synthesize raw intelligence into something a patient and their care team can actually act on.

The name EviGeno reflects this foundation directly: it is a contraction of Evidence and Genomics — a signal that every piece of intelligence we deliver is grounded in the patient's real clinical and molecular reality, not generic information that could apply to anyone.

The practice

EviGeno exists to close the gap between what patients are told is possible and what is actually available — helping people in late-stage illness find treatment options scientifically, rigorously, and matched to their actual individual situation. It operates as an independent research practice with no hospital affiliations, no pharmaceutical partnerships, and no referral arrangements of any kind. Every engagement is driven solely by what the evidence supports for that specific case.

Cases are taken on selectively — only when there is genuine reason to believe the research will add meaningful value. If a case is better served by a different resource, we say so plainly and point in the right direction.

"Every case is treated as the only case. That is not a tagline — it is the only way this kind of research can be done properly."

— Dexter Liu, Founder

Expertise

Three pillars, one practice

The research EviGeno produces sits at the intersection of three distinct domains — none of which alone is sufficient.

Clinical Genomics & NGS

Hands-on experience interpreting next-generation sequencing reports for oncology at Novogene. Fluent in the molecular language that determines treatment eligibility — mutations, variants, biomarkers, TMB, MSI, CNV, fusion events.

Oncology NGS report interpretation
Biomarker-to-therapy mapping
Trial eligibility criteria analysis
Rare disease genetic pathway review

Medical OSINT & Intelligence

Structured open-source intelligence methodology applied to the healthcare domain. Systematic extraction, cross-referencing, and validation of information across registries, regulatory filings, and scientific literature — including non-English and non-Western sources.

Multi-registry systematic search
Regulatory filing analysis (FDA / EMA)
Cross-language source coverage
Pipeline & biopharma intelligence

Global Regulatory Coverage

Deep familiarity with both Western and non-Western regulatory ecosystems — FDA, EMA, and beyond. Ability to access and interpret approval decisions, trial registrations, and pipeline data from sources that most Western researchers cannot effectively navigate.

FDA / EMA approval landscape
Non-Western regulatory ecosystems
Expanded access & compassionate use
Global biopharma pipeline tracking

Expert Network Affiliations

Verified subject-matter expert across leading global expert networks

GLG Guidepoint Dialectica Third Bridge

Philosophy & Ethics

How we think about this work

The principles that govern every engagement — not aspirational statements, but operational constraints.

Complete independence

EviGeno has no referral agreements with hospitals, no commercial relationships with pharmaceutical companies, and no financial incentive tied to any specific treatment outcome. The only criterion for what appears in a report is whether the evidence supports it for your specific case.

Information, not decisions

EviGeno provides structured intelligence — a map of what exists. Clinical decisions belong to the patient and their care team. We do not tell patients what to do. We tell them what is available, what the evidence shows, and what questions to bring to their oncologist.

Honesty about limits

Not every case has options that research can surface. When that is the honest conclusion, we say so — clearly, and with an explanation of what was searched and why the result is what it is. We do not manufacture hope where the evidence does not support it.

Strict confidentiality

All case information is held in strict confidence. Medical records, genomic data, and personal details are used solely for the purpose of your engagement and are never shared with, sold to, or disclosed to any third party under any circumstances.

Selective intake

Cases are accepted only when there is a genuine reason to believe research will add value. If your situation is better served by a different kind of resource — a patient advocacy organization, a hospital navigation service, or a direct specialist referral — we will say so on the intake call, before any payment is made.

The patient is the principal

Every engagement is structured around what is best for the patient — not what is easiest to research, most commercially interesting, or most likely to lead to follow-on work. The patient's situation, goals, and constraints define the scope of every engagement from the first call to the final report.

Get Started

Your case deserves
a complete picture.

Start with a free 20-minute intake call. No payment, no commitment — just a conversation to understand your case and confirm we can help.

We respond within 24 hours

Every inquiry is reviewed personally — no automated responses

Free 20-min intake call before any payment

We confirm fit before you commit to anything

Report delivered in 5–7 business days

Scope and timeline confirmed upfront for complex cases

Or reach out directly

[email protected]

Submit your case

We'll review your situation and be in touch within 24 hours.

Your information is kept strictly confidential and used only to respond to your inquiry. EviGeno does not share or sell personal data.