CASCADE: An Agentic Regulatory Network Framework for Patient-Data-Validated Downstream Perturbation Prediction
- URL: http://arxiv.org/abs/2608.05359v1
- Date: Wed, 05 Aug 2026 19:30:44 GMT
- Title: CASCADE: An Agentic Regulatory Network Framework for Patient-Data-Validated Downstream Perturbation Prediction
- Abstract summary: We use focal-gene copy-number amplification as a proxy for the inverse of knockdown against real TCGA patient tumor data.<n>For MYC, CASCADE's predicted knockdown targets show strong concordance with real amplified-vs-non-amplified tumor expression.<n>Its accuracy is not shown to exceed existing public knowledge of MYC- or E2F-driven biology.
- Score: 0.0
- License: http://creativecommons.org/licenses/by/4.0/
- Abstract: CASCADE is an agentic framework that predicts downstream transcriptional effects of gene perturbation from precomputed ARACNe regulatory networks, exposed via MCP. Prior work validates such tools by checking whether predicted genes are known cancer genes (membership); we instead test whether the predicted direction of change matches reality, using focal-gene copy-number amplification as a dosage-based proxy for the inverse of knockdown against real TCGA patient tumor data. For MYC, CASCADE's predicted knockdown targets show strong concordance with real amplified-vs-non-amplified tumor expression across three cancer types (BRCA: 90.0%, COAD: 72.0%, STAD: 85.7%; all p<0.0013), well above permutation baselines, surviving a PAM50 subtype control and replicating in an independent cohort (METABRIC, 87.2%). Compared against curated MSigDB gene-set baselines via Fisher's exact test, CASCADE's accuracy is not shown to exceed existing public knowledge of MYC- or E2F-driven biology, though its gene-specific direction-calling clearly outperforms a naive uniform guess. Extending to fifteen additional genes, validation proves gene-specific rather than universal: proliferation-machinery regulators mostly replicate, while lineage-identity transcription factors and one cyclin-D paralog (CCND2) consistently fail, a pattern we discuss as a hedged, post-hoc hypothesis. We separately benchmark whether an LLM-based agent correctly grounds natural-language requests into CASCADE's real MCP tool calls. Across 35 queries, a documented local model reaches 71.4% exact match (85.7% for a larger model); schema and gene-alias failures are resolved by scale or server-side correction, but both models confidently default to the wrong perturbation type on ambiguous queries, a failure a targeted fix could not resolve because its trigger condition never occurs.
Related papers
- Post-training Quantization for Hybrid Iterative Generative Models [52.791973512723324]
Iterative Generative Models (IGMs) span autoregressive and diffusion paradigms, and hybrid variants that couple them can achieve remarkable image-generation fidelity.<n>Post-training Quantization (PTQ) is appealing for acceleration, while directly applying vanilla PTQ to hybrid IGMs can trigger model collapse.<n>We introduce HyGenQ, a PTQ framework for hybrid IGMs.<n>It successfully quantizes representative hybrid IGMs to 8-bit precision (W8A8), significantly outperforming existing baselines and validating its robustness across different model families.
arXiv Detail & Related papers (2026-08-14T04:07:14Z) - Cross-Fitted Residual Utility for Primary-Preserving Cognitive Decision Correction in Automatic Modulation Classification [1.547549252134621]
We study a post-inference problem through cross-fitted residual utility and a primary-preserving cognitive decision policy.<n>A structured KAN-Fourier classifier supplies the default probability, while neural and non-neural candidates provide observable evidence.<n>On RMLA, RMLB, and HISAR, the complete system improves overall accuracy from 63.632% to 66.332%, 65.161% to 66.168%, and 77.769% to 79.867%.
arXiv Detail & Related papers (2026-08-03T11:07:37Z) - Modeling Normal Is All You Need: Joint Latent Clustering for Anomaly Detection in Multimodal Cyber-Physical Systems [47.027290803102666]
Normal behaviour is the union of many imbalanced, curved, thin-fringed operating regimes.<n>We model the normal law with a jointly learned latent representation plus explicit Gaussian-mixture mode clustering.<n>We evaluate under a deliberately fair protocol: raw point-wise metrics with no point adjustment, a trivial-detector difficulty split, prevalence-matched F1, and train-normal-only calibration.
arXiv Detail & Related papers (2026-07-07T10:10:00Z) - A self-evolving agent for explainable diagnosis of DFT-experiment band-gap mismatch [3.3602370127893724]
We introduce XDFT, a closed-loop agent that diagnoses the mismatch automatically.<n>On a verified benchmark of 124 materials, XDFT identifies a resolving mechanism for 70 of 90 mismatch cases.
arXiv Detail & Related papers (2026-04-29T14:11:03Z) - Information Fidelity in Tool-Using LLM Agents: A Martingale Analysis of the Model Context Protocol [69.11739400975445]
We introduce the first theoretical framework for analyzing error accumulation in Model Context Protocol (MCP) agents.<n>We show that cumulative distortion exhibits linear growth and high-probability deviations bounded by $O(sqrtT)$.<n>Key findings include: semantic weighting reduces distortion by 80%, and periodic re-grounding approximately every 9 steps suffices for error control.
arXiv Detail & Related papers (2026-02-10T21:08:53Z) - Prostate-VarBench: A Benchmark with Interpretable TabNet Framework for Prostate Cancer Variant Classification [14.190646211771073]
Variants of Uncertain Significance (VUS) limit the clinical utility of prostate cancer genomics.<n>Prostate-VarBench is a curated pipeline for creating prostate-specific benchmarks.
arXiv Detail & Related papers (2025-11-12T06:13:50Z) - DNABERT-2: Fine-Tuning a Genomic Language Model for Colorectal Gene Enhancer Classification [0.0]
DNABERT-2 is a transformer genomic language model that uses byte-pair encoding to learn variable-length tokens from DNA.<n>Gene enhancers control when and where genes switch on, yet their sequence diversity and tissue specificity make them hard to pinpoint in colorectal cancer.<n>This is the first study to apply a second-generation genomic language model with BPE tokenization to enhancer classification in colorectal cancer.
arXiv Detail & Related papers (2025-09-28T16:10:03Z) - Unlasting: Unpaired Single-Cell Multi-Perturbation Estimation by Dual Conditional Diffusion Implicit Bridges [68.98973318553983]
We propose a framework based on Dual Diffusion Implicit Bridges (DDIB) to learn the mapping between different data distributions.<n>We integrate gene regulatory network (GRN) information to propagate perturbation signals in a biologically meaningful way.<n>We also incorporate a masking mechanism to predict silent genes, improving the quality of generated profiles.
arXiv Detail & Related papers (2025-06-26T09:05:38Z) - CRTRE: Causal Rule Generation with Target Trial Emulation Framework [47.2836994469923]
We introduce a novel method called causal rule generation with target trial emulation framework (CRTRE)
CRTRE applies randomize trial design principles to estimate the causal effect of association rules.
We then incorporate such association rules for the downstream applications such as prediction of disease onsets.
arXiv Detail & Related papers (2024-11-10T02:40:06Z) - Using Pre-training and Interaction Modeling for ancestry-specific disease prediction in UK Biobank [69.90493129893112]
Recent genome-wide association studies (GWAS) have uncovered the genetic basis of complex traits, but show an under-representation of non-European descent individuals.
Here, we assess whether we can improve disease prediction across diverse ancestries using multiomic data.
arXiv Detail & Related papers (2024-04-26T16:39:50Z) - A Hybrid Machine Learning Model for Classifying Gene Mutations in Cancer using LSTM, BiLSTM, CNN, GRU, and GloVe [0.0]
We introduce a novel hybrid ensemble model that synergistically combines LSTM, BiLSTM, CNN, GRU, and GloVe embeddings for the classification of gene mutations in cancer.
Our approach achieved a training accuracy of 80.6%, precision of 81.6%, recall of 80.6%, and an F1 score of 83.1%, alongside a significantly reduced Mean Squared Error (MSE) of 2.596.
arXiv Detail & Related papers (2023-07-24T21:01:46Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.