Stars
A set of ready to use Agent Skills for research, science, engineering, analysis, finance and writing.
A curated list of awesome LLM and AI Agent Skills, resources and tools for customising AI Agent workflows - that works with Claude Code, Codex, Gemini CLI and your custom AI Agents
Code implementation of DeepRare (Nature 2026)
Data processing for and with foundation models! 🍎 🍋 🌽 ➡️ ➡️🍸 🍹 🍷
📖 NEW BOOK (/bin/zsh.99 launch): https://amzn.to/4cvxqSw — This repository showcases various advanced techniques for Retrieval-Augmented Generation (RAG) systems.
An automatic classification tool for PVS1 interpretation of null variants
PyGeneBe: A Python client seamlessly integrating with the GeneBe platform, offering efficient annotation of genetic variants through its API, while supporting pandas, VCF file formats, and HGVS par…
[WWW 2026] 🛠️ DeepAgent: A General Reasoning Agent with Scalable Toolsets
RAGFlow is a leading open-source Retrieval-Augmented Generation (RAG) engine that fuses cutting-edge RAG with Agent capabilities to create a superior context layer for LLMs
A virtual clinical environment for self‑evolving LLM diagnostic agents.
[3DV 2026] "SceneGen: Single-Image 3D Scene Generation in One Feedforward Pass"
The official code for "Boosting Pathology Foundation Models via Few-shot Prompt-tuning for Rare Cancer Subtyping"
Build and run agents you can see, understand and trust.
Website for checking the SpliceAI, Pangolin, and other predictor scores for variant(s) of interest.
Beyond the Model: Scaling Medical Capability with a Large Verifier System
An agentic RL framework to enhance retreival-augmented reasoning in Diagnostic Policy
Annotate models of genetic inheritance patterns in variant files (vcf files)
TradingAgents: Multi-Agents LLM Financial Trading Framework
Official code space for "SWE-Dev: Evaluating and Training Autonomous Feature-Driven Software Development"
A generalist foundation model for healthcare capable of handling diverse medical data modalities.
FGDD: An explainable dataset linking facial phenotypes and genes to rare genetic diseases
Call and score variants from WGS/WES of rare disease patients.
web-based analysis tool for rare disease genomics