AI-powered extracellular vesicle and exosome analysis for cancer biomarker discovery, liquid biopsy applications, and intercellular communication profiling.
BY FreedomIntelligenceUPDATED Oct 27, 2026
INTENDED FOR◈OpenClawInstall in a listed agent.
instructions.md
---
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
---
<!--
# COPYRIGHT NOTICE
# This file is part of the "Universal Biomedical Skills" project.
# Copyright (c) 2026 MD BABU MIA, PhD <md.babu.mia@mssm.edu>
# All Rights Reserved.
#
# This code is proprietary and confidential.
# Unauthorized copying of this file, via any medium is strictly prohibited.
#
# Provenance: Authenticated by MD BABU MIA
-->
# 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
| Type | Size | Origin | Markers |
|------|------|--------|---------|
| Exosomes | 30-150 nm | MVB fusion | CD9, CD63, CD81 |
| Microvesicles | 100-1000 nm | Membrane budding | Annexin V, ARF6 |
| Apoptotic bodies | 500-5000 nm | Cell death | Annexin V, PS |
| Large oncosomes | 1-10 μm | Tumor-specific | Variable |
## 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**:
```bash
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 Type | Elevated miRNAs | Clinical Use |
|-------------|-----------------|--------------|
| Pancreatic | miR-21, miR-17-5p, miR-155 | Early detection |
| Lung | miR-21, miR-126, miR-210 | Screening |
| Colorectal | miR-21, miR-92a, miR-29a | Detection |
| Prostate | miR-141, miR-375, miR-1290 | Prognosis |
| Ovarian | miR-21, miR-141, miR-200 family | Detection |
| Breast | miR-21, miR-155, miR-10b | Metastasis |
## EV Isolation Methods
| Method | Principle | Purity | Yield | Scalability |
|--------|-----------|--------|-------|-------------|
| Ultracentrifugation | Density | Moderate | High | Low |
| Size exclusion | Size | High | Moderate | Moderate |
| Immunocapture | Surface markers | Very high | Low | Low |
| Precipitation | Polymer | Low | Very high | High |
| Microfluidics | Various | Variable | Low | Low |
## 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 -->
---
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
---
<!--
# COPYRIGHT NOTICE
# This file is part of the "Universal Biomedical Skills" project.
# Copyright (c) 2026 MD BABU MIA, PhD <md.babu.mia@mssm.edu>
# All Rights Reserved.
#
# This code is proprietary and confidential.
# Unauthorized copying of this file, via any medium is strictly prohibited.
#
# Provenance: Authenticated by MD BABU MIA
-->
# 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
| Type | Size | Origin | Markers |
|------|------|--------|---------|
| Exosomes | 30-150 nm | MVB fusion | CD9, CD63, CD81 |
| Microvesicles | 100-1000 nm | Membrane budding | Annexin V, ARF6 |
| Apoptotic bodies | 500-5000 nm | Cell death | Annexin V, PS |
| Large oncosomes | 1-10 μm | Tumor-specific | Variable |
## 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**:
```bash
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 Type | Elevated miRNAs | Clinical Use |
|-------------|-----------------|--------------|
| Pancreatic | miR-21, miR-17-5p, miR-155 | Early detection |
| Lung | miR-21, miR-126, miR-210 | Screening |
| Colorectal | miR-21, miR-92a, miR-29a | Detection |
| Prostate | miR-141, miR-375, miR-1290 | Prognosis |
| Ovarian | miR-21, miR-141, miR-200 family | Detection |
| Breast | miR-21, miR-155, miR-10b | Metastasis |
## EV Isolation Methods
| Method | Principle | Purity | Yield | Scalability |
|--------|-----------|--------|-------|-------------|
| Ultracentrifugation | Density | Moderate | High | Low |
| Size exclusion | Size | High | Moderate | Moderate |
| Immunocapture | Surface markers | Very high | Low | Low |
| Precipitation | Polymer | Low | Very high | High |
| Microfluidics | Various | Variable | Low | Low |
## 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 -->
COMPATIBILITY & REFERENCES
Platform guidance
Imported from the listed AgentSkill.sh category. Complete supplied package files and notices are retained. Required external tools and credentials are not installed. No bundled code was executed during import. Individual agent task behavior has not been tested.
---name: liquid-biopsy-analytics-agent description: AI-powered comprehensive liquid biopsy analysis integrating ctDNA, CTCs, exosomes, and cfRNA for cancer detection, monitoring, and treatment guidance. license: MIT metadata: author: AI Group version: "1.0.0" created: "2026-01-19" compatibility:
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