---name: pan-cancer-multiomics-agent
description: AI-powered pan-cancer analysis integrating genomic, transcriptomic, proteomic, and epigenomic data for cancer subtyping, driver identification, and cross-cancer pattern discovery.
license: MIT
metadata:
author: AI Group
version: "1.0.0"
created: "2026-01-19"
compatibility:
- system: Python 3.10+
allowed-tools:
- run_shell_command
- read_file
- write_file
keywords:
- pan-cancer-multiomics-agent
- automation
- biomedical
measurable_outcome: execute task with >95% success rate.
---"
Pan-Cancer Multi-Omics Agent
The Pan-Cancer Multi-Omics Agent integrates multi-omics data across cancer types to identify shared oncogenic drivers, discover novel subtypes, and enable cross-cancer therapeutic insights. It leverages TCGA, CPTAC, and other pan-cancer resources with deep learning for comprehensive cancer characterization.
When to Use This Skill
- When analyzing patient tumors in context of pan-cancer molecular profiles.
- To identify shared drivers and vulnerabilities across cancer types.
- For discovering novel molecular subtypes that span histological boundaries.
- When prioritizing therapeutic targets with pan-cancer evidence.
- To benchmark single-cancer findings against pan-cancer patterns.
Core Capabilities
Pan-Cancer Subtyping: ML-based clustering across 32+ cancer types to identify molecular subtypes transcending tissue of origin.
Driver Discovery: Integrate mutation, expression, and CNV data to identify oncogenic drivers using pan-cancer statistical power.
Multi-Omics Fusion: Deep learning integration of mRNA, miRNA, methylation, and protein data for comprehensive profiles.
Pathway Analysis: Identify dysregulated pathways with pan-cancer prevalence and therapeutic implications.
Survival Modeling: PRISM framework for multi-omics prognostic marker discovery and survival prediction.
Therapeutic Matching: Map patient profiles to pan-cancer drug sensitivity data and clinical trial evidence.
TCGA Pan-Cancer Atlas Integration
| Data Type |
Samples |
Application |
| Somatic mutations |
11,000+ |
Driver identification |
| Copy number |
11,000+ |
Amplifications/deletions |
| mRNA expression |
11,000+ |
Expression subtypes |
| miRNA expression |
10,000+ |
Regulatory networks |
| DNA methylation |
10,000+ |
Epigenetic subtypes |
| Protein (RPPA) |
8,000+ |
Pathway activation |
Workflow
Input: Patient multi-omics data (mutations, CNV, expression, methylation).
Normalization: Harmonize data to TCGA reference standards.
Classification: Assign to pan-cancer molecular subtypes.
Driver Analysis: Identify patient-specific drivers in pan-cancer context.
Pathway Scoring: Calculate pathway activation scores.
Therapeutic Matching: Identify actionable targets and trial matches.
Output: Pan-cancer classification, driver report, pathway profiles, treatment recommendations.
Example Usage
User: "Classify this breast cancer patient's tumor in the pan-cancer context and identify shared drivers."
Agent Action:
python3 Skills/Oncology/Pan_Cancer_MultiOmics_Agent/pancancer_analyzer.py \
--mutations patient_mutations.maf \
--expression patient_rnaseq.tsv \
--methylation patient_methylation.tsv \
--cnv patient_cnv_segments.tsv \
--reference tcga_pancancer \
--subtype_method nmf_consensus \
--output pancancer_report/
Pan-Cancer Molecular Subtypes
Cross-cancer molecular taxonomy identifies patterns beyond histology:
| Subtype |
Characteristics |
Example Cancers |
| C1-Wound healing |
High proliferation, MYC amp |
Breast, ovarian, bladder |
| C2-IFN-gamma dominant |
Immune active, high TCR/BCR |
Melanoma, lung, cervical |
| C3-Inflammatory |
NF-kB, cytokine signatures |
Head/neck, stomach |
| C4-Lymphocyte depleted |
Low immune, PTEN loss |
Glioma, uveal melanoma |
| C5-Immunologically quiet |
Low expression overall |
Kidney chromophobe, thyroid |
| C6-TGF-beta dominant |
High TGF-B, fibrosis |
Pancreas, rectum, glioma |
Deep Learning Architecture
Multi-Omics Integration Model:
Input Layers:
- Genomic encoder (mutations, CNV)
- Transcriptomic encoder (mRNA, miRNA)
- Epigenomic encoder (methylation)
- Proteomic encoder (RPPA)
Fusion Layer:
- Cross-attention mechanism
- Multi-modal variational autoencoder
Output Heads:
- Subtype classifier
- Survival predictor
- Drug response predictor
MLOmics Database Access
The agent integrates with MLOmics, providing:
- 8,314 patient samples across 32 cancer types
- Pre-computed features for ML benchmarking
- Standardized train/test splits for reproducibility
- Drug sensitivity data for 300+ compounds
Prerequisites
- Python 3.10+
- PyTorch with multi-modal architectures
- Access to TCGA, CPTAC, or local data
- 16GB+ RAM for pan-cancer analysis
Related Skills
- Tumor_Clonal_Evolution - For intratumoral heterogeneity
- Multi_Omics_Integration - For single-patient integration
- Drug_Repurposing - For therapeutic matching
Clinical Applications
- Cancer of Unknown Primary (CUP): Identify tissue of origin
- Cross-indication trials: Find basket trial eligibility
- Driver prioritization: Pan-cancer functional evidence
- Prognosis: Multi-omics survival models
Author
AI Group - Biomedical AI Platform
1---2name: pan-cancer-multiomics-agent3description: ---name: pan-cancer-multiomics-agent4---5
6---name: pan-cancer-multiomics-agent
7description: AI-powered pan-cancer analysis integrating genomic, transcriptomic, proteomic, and epigenomic data for cancer subtyping, driver identification, and cross-cancer pattern discovery.
8license: MIT
9metadata:
10 author: AI Group
11 version: "1.0.0"
12 created: "2026-01-19"
13compatibility:
14 - system: Python 3.10+
15allowed-tools:
16 - run_shell_command
17 - read_file
18 - write_file
19
20keywords:
21 - pan-cancer-multiomics-agent
22 - automation
23 - biomedical
24measurable_outcome: execute task with >95% success rate.
25---"
26
27# Pan-Cancer Multi-Omics Agent
28
29The **Pan-Cancer Multi-Omics Agent** integrates multi-omics data across cancer types to identify shared oncogenic drivers, discover novel subtypes, and enable cross-cancer therapeutic insights. It leverages TCGA, CPTAC, and other pan-cancer resources with deep learning for comprehensive cancer characterization.
30
31## When to Use This Skill
32
33* When analyzing patient tumors in context of pan-cancer molecular profiles.
34* To identify shared drivers and vulnerabilities across cancer types.
35* For discovering novel molecular subtypes that span histological boundaries.
36* When prioritizing therapeutic targets with pan-cancer evidence.
37* To benchmark single-cancer findings against pan-cancer patterns.
38
39## Core Capabilities
40
411. **Pan-Cancer Subtyping**: ML-based clustering across 32+ cancer types to identify molecular subtypes transcending tissue of origin.
42
432. **Driver Discovery**: Integrate mutation, expression, and CNV data to identify oncogenic drivers using pan-cancer statistical power.
44
453. **Multi-Omics Fusion**: Deep learning integration of mRNA, miRNA, methylation, and protein data for comprehensive profiles.
46
474. **Pathway Analysis**: Identify dysregulated pathways with pan-cancer prevalence and therapeutic implications.
48
495. **Survival Modeling**: PRISM framework for multi-omics prognostic marker discovery and survival prediction.
50
516. **Therapeutic Matching**: Map patient profiles to pan-cancer drug sensitivity data and clinical trial evidence.
52
53## TCGA Pan-Cancer Atlas Integration
54
55| Data Type | Samples | Application |
56|-----------|---------|-------------|
57| Somatic mutations | 11,000+ | Driver identification |
58| Copy number | 11,000+ | Amplifications/deletions |
59| mRNA expression | 11,000+ | Expression subtypes |
60| miRNA expression | 10,000+ | Regulatory networks |
61| DNA methylation | 10,000+ | Epigenetic subtypes |
62| Protein (RPPA) | 8,000+ | Pathway activation |
63
64## Workflow
65
661. **Input**: Patient multi-omics data (mutations, CNV, expression, methylation).
67
682. **Normalization**: Harmonize data to TCGA reference standards.
69
703. **Classification**: Assign to pan-cancer molecular subtypes.
71
724. **Driver Analysis**: Identify patient-specific drivers in pan-cancer context.
73
745. **Pathway Scoring**: Calculate pathway activation scores.
75
766. **Therapeutic Matching**: Identify actionable targets and trial matches.
77
787. **Output**: Pan-cancer classification, driver report, pathway profiles, treatment recommendations.
79
80## Example Usage
81
82**User**: "Classify this breast cancer patient's tumor in the pan-cancer context and identify shared drivers."
83
84**Agent Action**:
85```bash
86python3 Skills/Oncology/Pan_Cancer_MultiOmics_Agent/pancancer_analyzer.py \
87 --mutations patient_mutations.maf \
88 --expression patient_rnaseq.tsv \
89 --methylation patient_methylation.tsv \
90 --cnv patient_cnv_segments.tsv \
91 --reference tcga_pancancer \
92 --subtype_method nmf_consensus \
93 --output pancancer_report/
94```
95
96## Pan-Cancer Molecular Subtypes
97
98Cross-cancer molecular taxonomy identifies patterns beyond histology:
99
100| Subtype | Characteristics | Example Cancers |
101|---------|-----------------|-----------------|
102| C1-Wound healing | High proliferation, MYC amp | Breast, ovarian, bladder |
103| C2-IFN-gamma dominant | Immune active, high TCR/BCR | Melanoma, lung, cervical |
104| C3-Inflammatory | NF-kB, cytokine signatures | Head/neck, stomach |
105| C4-Lymphocyte depleted | Low immune, PTEN loss | Glioma, uveal melanoma |
106| C5-Immunologically quiet | Low expression overall | Kidney chromophobe, thyroid |
107| C6-TGF-beta dominant | High TGF-B, fibrosis | Pancreas, rectum, glioma |
108
109## Deep Learning Architecture
110
111**Multi-Omics Integration Model**:
112```
113Input Layers:
114 - Genomic encoder (mutations, CNV)
115 - Transcriptomic encoder (mRNA, miRNA)
116 - Epigenomic encoder (methylation)
117 - Proteomic encoder (RPPA)
118
119Fusion Layer:
120 - Cross-attention mechanism
121 - Multi-modal variational autoencoder
122
123Output Heads:
124 - Subtype classifier
125 - Survival predictor
126 - Drug response predictor
127```
128
129## MLOmics Database Access
130
131The agent integrates with MLOmics, providing:
132- 8,314 patient samples across 32 cancer types
133- Pre-computed features for ML benchmarking
134- Standardized train/test splits for reproducibility
135- Drug sensitivity data for 300+ compounds
136
137## Prerequisites
138
139* Python 3.10+
140* PyTorch with multi-modal architectures
141* Access to TCGA, CPTAC, or local data
142* 16GB+ RAM for pan-cancer analysis
143
144## Related Skills
145
146* Tumor_Clonal_Evolution - For intratumoral heterogeneity
147* Multi_Omics_Integration - For single-patient integration
148* Drug_Repurposing - For therapeutic matching
149
150## Clinical Applications
151
1521. **Cancer of Unknown Primary (CUP)**: Identify tissue of origin
1532. **Cross-indication trials**: Find basket trial eligibility
1543. **Driver prioritization**: Pan-cancer functional evidence
1554. **Prognosis**: Multi-omics survival models
156
157## Author
158
159AI Group - Biomedical AI Platform