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Ultra-Precision Neurology

Molecular Precision Neuro-Stratification

PathoBrainSeq extracts blood cells from patients and uses Whole Genome Sequencing (WGS) and single-cell RNA sequencing (scRNA-seq) to achieve ultra-precision diagnosis of brain diseases — identifying what other platforms cannot.

🔬 PILOT DATASET — ONGOING RESEARCH
4
Non-AD Controls
4
Early AD Patients
3
Late AD Patients
AD Alzheimer's DEMENTIA Dementia PD Parkinson's HD Huntington's ALS ALS PRION Prion Disease

Blood Cell → Brain Disease Diagnosis Pipeline

From a simple blood draw, we extract immune cells and apply WGS and scRNA-seq to detect molecular signatures of neurodegeneration — years before clinical symptoms appear.

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Blood Draw
Patient sample
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Cell Isolation
PBMCs / immune cells
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WGS
Whole Genome Sequencing
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scRNA-seq
Single-cell transcriptomics
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AI Analysis
Bioinformatics pipeline
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Precision Report
Personalized insights
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WGS: Mutation Detection
Identifies disease-causing genetic variants (APOE ε4, LRRK2, HTT CAG repeats) with whole-genome resolution
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scRNA-seq: Disease Progression
Tracks transcriptomic changes at single-cell resolution — detecting disease progression before clinical symptoms emerge
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Precision Drug Management
Personalised drug response profiling to guide prescription decisions and monitor treatment efficacy over time

Personal, Proactive, and Precise

Our platform integrates multi-omics data with digital biomarker testing to deliver the most comprehensive neurological health picture available.

1
Blood-Based Genomics
WGS identifies disease-risk mutations. scRNA-seq tracks real-time transcriptomic changes in individual immune cells — providing unprecedented molecular resolution.
2
Digital Cognitive Assessment
The mNeuroMap app provides online-based screening to quickly classify brain disease categories — serving as a preliminary step before NeuroMap precision genomic diagnostics.
3
Integrated Precision Report
Genomic + transcriptomic + digital biomarker data are integrated into a unified report — enabling precise, personalized clinical decisions.
$296B
mHealth Market by 2030
19%
CAGR — Digital Neurology
11
Pilot Dataset (ongoing)
4 control, 4 early AD, 3 late AD
6
Brain Diseases Targeted

What Makes Us Different

The first platform to combine WGS + scRNA-seq + digital biomarkers for multi-disease neurological profiling.

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WGS Mutation Profiling
Whole genome sequencing detects rare and common disease-causing variants across all 6 billion base pairs — providing unmatched genetic resolution for neurological risk.
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scRNA-seq Disease Monitoring
Single-cell RNA sequencing tracks disease progression at the individual cell level — capturing transcriptomic changes that predict clinical decline before symptoms appear.
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mNeuroMap Digital Platform
Online-based screening platform for quickly checking multiple brain disease categories — a preliminary classification tool for NeuroMap precision diagnostics.
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Precision Drug Management
Pharmacogenomic profiling guides drug prescription decisions — identifying which patients will respond to specific treatments and monitoring efficacy over time.
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Drug Development Support
Our multi-omics biomarker data helps pharmaceutical companies identify patient responders earlier — addressing the chronic failure rate in neurological drug development.
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Data Privacy
We are committed to protecting your data as we build our platform. Security and privacy are core to our architecture from day one.

Why the World Needs PathoBrainSeq

We are in pre-launch phase. These are the transformative impacts we anticipate — and that scientists, clinicians, and advocates are eagerly awaiting.

"A platform that combines WGS and scRNA-seq data with longitudinal digital biomarkers could finally give us the molecular precision we need to match patients to therapies — something that has eluded neurology for decades."
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Neurological Drug Development
Anticipated impact on clinical trials
"We have seen too many Alzheimer's drugs fail in Phase III because we selected the wrong patients. A multi-omics approach identifying responders at the molecular level before treatment could transform the success rate of neuro drug development."
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Pharmaceutical Research
Anticipated impact on drug failure rates
"For families watching a loved one decline, early molecular detection and precise prescription management could mean the difference between years of quality life and accelerated decline. This is the innovation our community needs."
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Patient & Caregiver Community
Anticipated patient benefit
📱 Digital Assessment Platform

mNeuroMap App

Online-based brain disease screening tool — quickly classify neurodegenerative disease categories before in-depth NeuroMap genomic analysis.

🚀 Launch mNeuroMap App

Multi-Disease Assessment Platform

Select your disease focus, complete a battery of validated digital biomarker tests, and track results longitudinally. Designed for patients, caregivers, and healthcare providers.

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Patient Mode
Personal dashboard, monthly score tracking, 30-day rolling averages, profile photo, and PathoBrainSeq genetic data integration.
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Caregiver Mode
Monitor your linked patient's results in real-time. Receive alerts when scores drop below threshold. View longitudinal trends and share PDF reports.
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Provider Mode
Patient list management, detailed longitudinal dashboards, APOE status integration, PDF export, and clinical alert notifications.
Alzheimer's Disease — AD ● Live
Comprehensive AD Biomarker Assessment
Episodic memory, visuospatial navigation, language, executive function, and digital motor biomarkers — combined with APOE genetic status for the most complete early-detection battery available.
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Cognitive (MoCA/MMSE-based)
Episodic memory · Working memory · Orientation · Language
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Visuospatial / Executive
Pattern recognition · Spatial reasoning · Serial subtraction
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Digital Biomarkers
Finger tapping speed · Stroop interference · Word recall
🧬 Genetics
APOE ε4 Status Integration
WGS-derived APOE genotype displayed alongside cognitive scores for integrated risk assessment
📊 Tool
MoCA-aligned Battery
Orientation, memory, attention, language, and visuospatial — aligned to Montreal Cognitive Assessment domains
🏃 Motor
Finger Tapping Speed
10-second digital tapping test measuring bradykinesia — a key early AD neuromotor biomarker
Dementia — General ● Live
Broad Dementia Cognitive Screen
A comprehensive screening battery covering all major dementia subtypes — including vascular, Lewy body, and frontotemporal. Includes MMSE-aligned questions and multi-gene risk scoring.
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Orientation & Memory
Temporal orientation · Delayed recall · Attention
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Language & Executive
Verbal fluency · Serial subtraction · Naming
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Functional Assessment
ADL questionnaire · Behavioural change screen
📊 Tool
MMSE / SLUMS Battery
Mini-Mental State Exam and Saint Louis University Mental Status aligned screening
🔬 Genomics
Multi-gene Risk Panel
WGS-based polygenic risk scoring across APOE, CLU, BIN1, and CR1 loci
Parkinson's Disease — PD ● In Development
Motor & Cognitive PD Battery
Integrates MoCA cognitive testing with finger tapping, spiral drawing, and LRRK2/GBA genetic variant detection for the most comprehensive PD biomarker profile.
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Motor Assessment
Finger tapping · Spiral drawing · Gait analysis
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Non-Motor Symptoms
Sleep quality · Smell assessment · Autonomic screen
🧬 Genetics
LRRK2 / GBA / SNCA Panel
WGS-derived PD-specific variant analysis — in development
Huntington's Disease — HD ● In Development
HD Comprehensive Assessment
Processing speed, oculomotor function, and HTT CAG repeat analysis. Behavioural change screening for early HD detection and progression monitoring.
Processing Speed
Stroop test · Reaction time · Serial 7s
🧬 Genetics
HTT CAG Repeat Analysis
Definitive HD genetic test via WGS — in development
ALS (Lou Gehrig's) ● In Development
ALS Digital Biomarker Screen
Motor neuron decline tracking, speech pattern analysis, limb strength assessment, and SOD1/C9orf72 genetic panel for comprehensive ALS biomarker profiling.
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Motor Neuron Function
Grip strength proxy · Speech analysis · Breathing screen
🧬 Genetics
SOD1 / C9orf72 Panel
ALS-associated genetic variants via WGS — in development
Prion Disease ● In Development
Prion Disease Progression Tracking
Rapid functional decline monitoring, cerebellar function, myoclonus screening, and prion-specific biomarker tracking for early detection of prion disease progression.
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Rapid Decline Monitoring
Velocity scoring · Cerebellar function · Myoclonus
🧬 Genetics
PRNP Gene Analysis
Prion protein gene variant detection — in development
📋 Service Status

What's Available Now

PathoBrainSeq is in active research and pre-commercial phase. We are transparent about what is live, what is in development, and what's on our roadmap.

● LIVE NOW

Alzheimer's Disease & Dementia — Active Services

Our current pilot dataset includes 3 non-AD controls, 4 early AD, and 3 late AD patients. We are actively accepting research collaborations, pilot study partnerships, and early clinical inquiries for AD and Dementia screening.

✅ Available
WGS-based AD Genetic Panel
APOE ε4, APP, PSEN1/2 variant analysis from blood
✅ Available
scRNA-seq Progression Monitoring
Disease progression tracking at single-cell resolution
✅ Available
mNeuroMap Digital Assessment
Web-based cognitive & motor biomarker testing
⚙️ IN DEVELOPMENT

Parkinson's & Huntington's

Motor biomarker validation, LRRK2/GBA/HTT genetic panel development, and scRNA-seq signature identification ongoing.

  • ⚙️ Motor biomarker protocols in validation
  • ⚙️ Genetic panel design complete — testing phase
  • ⚙️ ETA: Research partnerships open now
🗺️ ROADMAP

ALS & Prion Disease

Planned for Phase 2 expansion following core AD/PD/HD platform validation and series A funding.

  • 🗺️ SOD1/C9orf72 panel (ALS) — planned
  • 🗺️ PRNP analysis (Prion) — planned
  • 🗺️ Global market expansion planned
🧬 Request NeuroMap Services
Whether you're a clinician, researcher, or institution — contact us to discuss NeuroMap blood-based genomic testing, research partnerships, or pilot study participation.
🧬 NeuroMap

NeuroMap — Blood-Based Early Precision Diagnostics

Early precision diagnosis of neurodegenerative diseases through blood-based WGS & scRNA-seq genomic analysis — detecting disease-causing mutations and monitoring progression before symptoms appear.

Whole Genome Sequencing

WGS provides comprehensive coverage of the entire genome — detecting disease-causing mutations, structural variants, and pharmacogenomic markers that targeted panels miss.

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AD Mutation Panel (WGS)
APOE ε4 genotyping, APP, PSEN1, PSEN2 rare variant detection, and polygenic risk scoring across 75+ AD-associated loci. Identifies both monogenic and complex genetic risk.
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PD/HD Genetic Panels (WGS)
LRRK2, SNCA, GBA, PINK1 for Parkinson's. HTT CAG repeat expansion analysis for Huntington's — the definitive genetic test. In development phase.
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Pharmacogenomics (WGS)
Identifies which patients will respond to specific AD/PD drugs — guiding prescription decisions and helping pharmaceutical companies select responders for clinical trials.

Single-Cell RNA Sequencing

scRNA-seq goes beyond genetics — measuring which genes are actually active in each individual cell at the time of sampling, revealing disease progression dynamics invisible to WGS.

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Disease Progression Monitoring
Sequential scRNA-seq samples reveal transcriptomic changes over time — tracking neuroinflammatory signatures, microglial activation, and synaptic gene expression changes as disease progresses.
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Cell-Type-Specific Signatures
Identifies which specific immune cell populations are dysregulated in each patient — providing cell-resolution insights that bulk RNA-seq cannot deliver.
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Treatment Response Tracking
Pre- and post-treatment scRNA-seq reveals molecular response to therapy at single-cell resolution — enabling precision monitoring of drug efficacy and early detection of non-response.
📬 Request NeuroMap Services
Ready to discuss blood-based WGS, scRNA-seq, or integrated multi-omics early precision diagnostics? Leave your contact below and our team will reach out within 24 hours.
👥 Our Team

About PathoBrainSeq

A team of seasoned neuroscientists, bioinformaticians, and clinicians united by a mission to revolutionize brain disease diagnosis.

Precise Diagnosis for Personalized Medicine

We believe that ultra-precision neurological diagnostics — combining WGS, scRNA-seq, and digital biomarkers — should be accessible to patients and clinicians everywhere.

Brain diseases like Alzheimer's have seen decades of drug development failures — primarily because we haven't had the molecular tools to select the right patients. PathoBrainSeq is building those tools.

The Gap We Fill

Single-disease platforms — existing tools address only one condition at a time
No transcriptomics — genetic panels miss dynamic disease progression signals
Digital-genomics gap — cognitive apps and genetic tests are siloed, not integrated
PathoBrainSeq solves all three — WGS + scRNA-seq + digital biomarkers, integrated

Experienced. Multidisciplinary. Driven.

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Leadership
Chief Executive Officer
CEO
Neuroscience Expert
20 Years of Brain Disease Research
Two decades dedicated to neurodegenerative disease research — spanning molecular mechanisms, translational biomarker development, and clinical trial design for Alzheimer's and related dementias. Founded PathoBrainSeq to bridge the gap between genomic discovery and clinical diagnostics.
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Technology
Chief Technology Officer
CTO
Bioinformatics Expert
Computer Science + 15 Years Bioinformatics
Computer Science foundation with 15 years of applied bioinformatics experience — building large-scale genomics pipelines, WGS analysis workflows, and scRNA-seq processing platforms. Architect of PathoBrainSeq's multi-omics analytical infrastructure.
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Science
Chief Science Officer
CSO
Academic Neuroscientist
Professor & 15-Year Brain Disease Researcher
Full professor at a leading research institution, with 15 years of focused brain disease research and an extensive publication record in neurodegeneration. Brings rigorous academic standards and cutting-edge scientific expertise to PathoBrainSeq's research agenda.
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Clinical
Clinical Advisory Board
CAB
US & Korean Medical Board Physicians
Clinical Advisors — US & South Korea
Our Clinical Advisory Board comprises board-certified physicians from both the United States and South Korea — actively caring for neurological patients in clinical practice. They provide real-world clinical validation, patient insights, and regulatory guidance for both US FDA and Korean MFDS pathways.
📬 Get In Touch

Contact PathoBrainSeq

Whether you're a patient, clinician, researcher, pharma partner, or investor — we want to hear from you.

Let's Connect

We're building the future of neuro-diagnostics — and we need collaborators, patients, clinicians, and partners. Every conversation matters.

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USA
United States — Research & Clinical Partnerships
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Korea
South Korea — Clinical Advisory & Regulatory
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For Clinicians
B2B clinical integration, pilot programs, EHR API
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For Researchers
Multi-omics data collaboration, biomarker validation
Send Us a Message
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