OpenClaw-Medical-Skills exosome-ev-analysis-agent

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install
source · Clone the upstream repo
git clone https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills
Claude Code · Install into ~/.claude/skills/
T=$(mktemp -d) && git clone --depth=1 https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills "$T" && mkdir -p ~/.claude/skills && cp -r "$T/skills/exosome-ev-analysis-agent" ~/.claude/skills/freedomintelligence-openclaw-medical-skills-exosome-ev-analysis-agent && rm -rf "$T"
OpenClaw · Install into ~/.openclaw/skills/
T=$(mktemp -d) && git clone --depth=1 https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills "$T" && mkdir -p ~/.openclaw/skills && cp -r "$T/skills/exosome-ev-analysis-agent" ~/.openclaw/skills/freedomintelligence-openclaw-medical-skills-exosome-ev-analysis-agent && rm -rf "$T"
manifest: skills/exosome-ev-analysis-agent/SKILL.md
source content
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name: 'exosome-ev-analysis-agent' description: 'AI-powered extracellular vesicle and exosome analysis for cancer biomarker discovery, liquid biopsy applications, and intercellular communication profiling.' measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools:

  • read_file
  • run_shell_command

Exosome/EV Analysis Agent

The Exosome/EV Analysis Agent provides comprehensive AI-driven analysis of extracellular vesicles for cancer biomarker discovery, liquid biopsy applications, and tumor-microenvironment communication profiling.

When to Use This Skill

  • When analyzing exosome cargo (RNA, protein, lipids) for biomarker discovery.
  • To identify tumor-derived EVs in liquid biopsy samples.
  • For profiling EV-mediated intercellular communication in cancer.
  • When predicting EV uptake and functional effects on recipient cells.
  • To design EV-based diagnostic or therapeutic applications.

Core Capabilities

  1. EV Cargo Profiling: Analyze exosomal RNA (miRNA, lncRNA, circRNA), proteins, and lipids.

  2. Tumor EV Identification: Distinguish tumor-derived EVs from normal EVs using surface markers and cargo.

  3. Biomarker Discovery: ML-driven identification of cancer-specific EV signatures.

  4. Communication Network: Map EV-mediated signaling between tumor and TME cells.

  5. Functional Prediction: Predict downstream effects of EV cargo on recipient cells.

  6. Diagnostic Development: Support EV-based diagnostic assay design.

EV Classification

TypeSizeOriginMarkers
Exosomes30-150 nmMVB fusionCD9, CD63, CD81
Microvesicles100-1000 nmMembrane buddingAnnexin V, ARF6
Apoptotic bodies500-5000 nmCell deathAnnexin V, PS
Large oncosomes1-10 μmTumor-specificVariable

Workflow

  1. Input: EV isolation method, cargo profiling data (RNA-seq, proteomics), characterization data.

  2. Quality Assessment: Evaluate EV purity and characterization (NTA, TEM, markers).

  3. Cargo Analysis: Profile RNA, protein, and lipid content.

  4. Source Deconvolution: Identify tumor vs stromal EV origin.

  5. Biomarker Selection: Identify cancer-specific signatures.

  6. Functional Prediction: Predict effects on recipient cells.

  7. Output: EV profile, biomarker candidates, functional predictions.

Example Usage

User: "Analyze exosomal miRNA profiles from plasma samples to identify pancreatic cancer biomarkers."

Agent Action:

python3 Skills/Oncology/Exosome_EV_Analysis_Agent/ev_analyzer.py \
    --ev_mirna exosome_smallrna.tsv \
    --ev_protein exosome_proteome.tsv \
    --sample_groups pancreatic_cancer,healthy \
    --normalization spike_in \
    --biomarker_discovery true \
    --output ev_biomarker_report/

Exosomal miRNA Cancer Biomarkers

Cancer TypeElevated miRNAsClinical Use
PancreaticmiR-21, miR-17-5p, miR-155Early detection
LungmiR-21, miR-126, miR-210Screening
ColorectalmiR-21, miR-92a, miR-29aDetection
ProstatemiR-141, miR-375, miR-1290Prognosis
OvarianmiR-21, miR-141, miR-200 familyDetection
BreastmiR-21, miR-155, miR-10bMetastasis

EV Isolation Methods

MethodPrinciplePurityYieldScalability
UltracentrifugationDensityModerateHighLow
Size exclusionSizeHighModerateModerate
ImmunocaptureSurface markersVery highLowLow
PrecipitationPolymerLowVery highHigh
MicrofluidicsVariousVariableLowLow

AI/ML Components

Biomarker Discovery:

  • Differential expression analysis
  • Machine learning feature selection
  • Multi-marker panel optimization
  • Cross-validation and independent validation

Source Deconvolution:

  • Marker-based classification
  • ML models for tumor vs normal EVs
  • Cell-type specific cargo signatures

Functional Prediction:

  • miRNA target prediction
  • Pathway enrichment
  • Recipient cell effect modeling

EV Characterization Quality

MISEV Guidelines Requirements:

  • Particle concentration (NTA/TRPS)
  • Size distribution (NTA/DLS/TEM)
  • Protein markers (CD9/63/81, TSG101, ALIX)
  • Negative markers (calnexin, albumin)
  • Morphology (TEM)

Clinical Applications

  1. Early Detection: Cancer screening from blood EVs
  2. Prognosis: EV signatures predicting outcomes
  3. Therapy Response: Monitor treatment effect
  4. Metastasis: Predict metastatic potential
  5. Resistance: Identify resistance mechanisms

Prerequisites

  • Python 3.10+
  • Small RNA analysis tools
  • Proteomics analysis packages
  • ML frameworks (scikit-learn, XGBoost)

Related Skills

  • Liquid_Biopsy_Analytics_Agent - For other liquid biopsy analytes
  • Tumor_Microenvironment - For TME communication
  • Cell-Free RNA Analysis - For plasma RNA

Emerging Applications

  1. EV-based Drug Delivery: Therapeutic cargo loading
  2. EV Engineering: Surface modification for targeting
  3. Tumor Vaccines: EV-based immunotherapy
  4. Companion Diagnostics: Treatment selection markers

Author

AI Group - Biomedical AI Platform

<!-- AUTHOR_SIGNATURE: 9a7f3c2e-MD-BABU-MIA-2026-MSSM-SECURE -->