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promptadmin e22c861d46 [upstream-sync] README.md from ai-boost/awesome-ai-for-science@4afd72ec [catalogue] 2026-07-07 20:18:40 +00:00
promptadmin bf0d468978 Merge upstream-sync branch upstream-sync/awesome-ai-for-science-20260706-e0df96-elsa
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promptadmin e2d27fc52e Merge pull request '[Upstream sync] ai-boost/awesome-ai-for-science (github) — 0 added, 1 modified' (#31) from upstream-sync/awesome-ai-for-science-20260705-99a575-uivu into main
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promptadmin 21abde0feb [upstream-sync] README.md from ai-boost/awesome-ai-for-science@99a57577 [catalogue] 2026-07-05 20:08:20 +00:00
promptadmin 55837bb543 [upstream-sync] README.md from ai-boost/awesome-ai-for-science@cf74319a [catalogue] 2026-07-04 19:58:44 +00:00
promptadmin bfc772b9f6 [upstream-sync] README.md from ai-boost/awesome-ai-for-science@9f62d8a3 [catalogue] 2026-07-04 13:57:30 +00:00
promptadmin 168b1b0083 [upstream-sync] README.md from ai-boost/awesome-ai-for-science@cca0924c [catalogue] 2026-07-04 07:56:14 +00:00
promptadmin 7fd95fb00f [upstream-sync] README.md from ai-boost/awesome-ai-for-science@86c5f147 [catalogue] 2026-07-03 19:54:17 +00:00
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title: "Readme"
task: ""
lineage_type: import
upstream_source: https://github.com/ai-boost/awesome-ai-for-science/blob/e0df96d7/README.md
upstream_sha: e0df96d7
imported_at: 2026-07-06
upstream_source: https://github.com/ai-boost/awesome-ai-for-science/blob/4afd72ec/README.md
upstream_sha: 4afd72ec
imported_at: 2026-07-07
prompt_class: catalogue
upstream_changes: accepted
author: upstream
@@ -592,6 +592,7 @@ validated: false
- [AlphaMissense](https://github.com/google-deepmind/alphamissense) - Google DeepMind's AlphaFold-derived classifier for proteome-wide missense variant effect prediction, providing pathogenicity scores for all ~71M possible human missense variants and classifying 89% with 90% precision; pre-computed predictions are integrated into Ensembl VEP and UCSC Genome Browser to support clinical variant interpretation (Science 2023)
- [AlphaGenome](https://github.com/google-deepmind/alphagenome) - Google DeepMind's unified DNA sequence foundation model predicting molecular consequences of genetic variants from single-base resolution up to 1 megabase context, jointly outputting thousands of regulatory tracks (RNA expression, splicing, chromatin accessibility, TF binding, contact maps) for human and mouse genomes via a Python client and non-commercial API (2025)
- [GPN-Star (Song Lab, UC Berkeley, bioRxiv 2025)](https://github.com/songlab-cal/gpn) - Phylogeny-aware genomic language model trained on whole-genome alignments across multiple evolutionary timescales, predicting functional constraints and variant effects for human, mouse, chicken, fly, worm, and Arabidopsis genomes (344+ stars, MIT License)
- [GENERanno (bioRxiv 2025)](https://github.com/GenerTeam/GENERanno) - Genomic foundation model for metagenomic and genome annotation, featuring an 8k base-pair context and 500M parameters trained on 386B base pairs of eukaryotic DNA; provides expert models and a unified CLI for prokaryotic/eukaryotic coding-sequence annotation with strong performance on Genomic Benchmarks, Nucleotide Transformer tasks, and custom Gener tasks (GenerTeam, 314+ stars, MIT License)
- [DeepVariant](https://github.com/google/deepvariant) - Google DeepMind's deep learning analysis pipeline for calling genetic variants (SNPs and indels) from next-generation DNA sequencing data, achieving human expert-level accuracy and widely adopted in clinical genomics, population genetics, and precision medicine; pre-trained models available for multiple sequencing platforms and organismal genomes (Nature Biotechnology 2018, 3.7K+ stars)
- [Casanovo](https://github.com/Noble-Lab/casanovo) - Transformer encoder-decoder for de novo peptide sequencing from tandem mass spectrometry, translating MS/MS spectra directly to peptide sequences without reference databases, enabling identification of novel peptides for immunopeptidomics, antibody repertoires, and metaproteomes (Noble Lab UW, Nature Communications 2024)
@@ -617,6 +618,7 @@ validated: false
- [PLIP (Nature Medicine 2023)](https://github.com/PathologyFoundation/plip) - First vision-and-language foundation model for pathology AI, fine-tuned from CLIP on 249K image-caption pairs, enabling open-ended visual-semantic search and zero-shot diagnosis across histopathology (Pathology Foundation, 376+ stars)
- [TITAN (Nature Medicine 2024)](https://github.com/mahmoodlab/TITAN) - Multimodal whole-slide pathology foundation model jointly pretrained on H&E histology and diagnostic text reports, enabling zero-shot cancer subtyping, biomarker prediction, and multimodal reasoning across diverse cancer types (Mahmood Lab, 341+ stars)
- [Virchow (Nature Medicine 2024)](https://huggingface.co/paige-ai/Virchow) - Self-supervised pathology foundation model (ViT-Huge, 632M parameters) pretrained via DINOv2 on 1.5M whole-slide images from Memorial Sloan Kettering across 17 cancer types, with Virchow2 follow-up scaling to 3.1M slides and mixed magnifications, achieving SOTA on biomarker prediction, mutation classification, and rare cancer detection (Paige AI & MSK)
- [H-Optimus (Bioptimus, Nature Medicine 2025)](https://huggingface.co/bioptimus/H-optimus-0) - Open-weights pathology foundation model family (H-Optimus-0: 1.1B-parameter ViT pretrained via DINOv2 on 500M+ diagnostic image tiles; H-Optimus-1 follow-up) for whole-slide image analysis, achieving strong zero-shot and fine-tuned transfer across biomarker prediction, cancer subtyping, and mutation classification (Bioptimus, Apache 2.0)
- [TRIDENT (2025)](https://github.com/mahmoodlab/TRIDENT) - Toolkit for large-scale whole-slide image processing supporting 22+ patch encoders (UNI, CONCH, Virchow, H-Optimus-0, etc.), slide encoders (TITAN, GigaPath, PRISM, CHIEF, Madeleine, Feather), tissue segmentation, and multi-GPU inference with end-to-end pipeline and smart resume for standardized deployment of computational pathology foundation models (Mahmood Lab, Harvard Medical School, 553+ stars)
- [Feather (Mahmood Lab, ICML 2025 Spotlight)](https://github.com/mahmoodlab/MIL-Lab) - Lightweight supervised slide foundation model with 0.9M parameters pretrained on 24K whole-slide images for pan-cancer morphological classification, achieving competitive performance with much larger self-supervised models (TITAN, GigaPath) while enabling finetuning on consumer-grade GPUs; includes standardized MIL implementations and benchmarking across 15+ classification tasks (Mahmood Lab, Harvard Medical School, 153+ stars)
- [PathChat (Nature Medicine 2024)](https://github.com/MahmoodLab/PathChat) - Multimodal generative AI assistant for computational pathology enabling interactive visual-language conversations over histopathology images for diagnostic reasoning, case discussion, and education, built on a Mistral-7B backbone with domain-specific fine-tuning (Mahmood Lab, Harvard Medical School, 1.2K+ stars)
@@ -847,6 +849,7 @@ validated: false
- [DiffEqFlux.jl](https://github.com/SciML/DiffEqFlux.jl) - Neural ordinary differential equations with O(1) backprop and GPU support (900+ stars)
- [Optimization.jl](https://github.com/SciML/Optimization.jl) - Unified interface for local, global, gradient-based and derivative-free optimization (800+ stars)
- [PaddleScience](https://github.com/PaddlePaddle/PaddleScience) - SDK & library for AI-driven scientific computing applications
- [Tesseract Core (Pasteur Labs, SciPy 2025 / JOSS)](https://github.com/pasteurlabs/tesseract-core) - Universal components for differentiable scientific computing, packaging heterogeneous scientific tools into self-contained, portable, gradient-propagating components with auto-generated schemas, CLI/REST API/Python SDK interfaces, and reproducible deployment across local, cloud, and HPC environments (105+ stars, Apache 2.0)
- [Flux.jl](https://github.com/FluxML/Flux.jl) - Machine learning in Julia
### Specialized Frameworks