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fastVEP: High-performance Variant Effect Predictor in Rust
AI agents running research on single-GPU nanochat training automatically
miolini / autoresearch-macos
Forked from karpathy/autoresearchAI agents running research on single-GPU nanochat training automatically adopted for MacOS
👻 Ghostty is a fast, feature-rich, and cross-platform terminal emulator that uses platform-native UI and GPU acceleration.
A concise, beginner-friendly introduction to the core ideas of linear algebra.
A DSL for data-driven computational pipelines
Implement a ChatGPT-like LLM in PyTorch from scratch, step by step
Copy number variant detection from targeted DNA sequencing
Pangolin is a deep-learning method for predicting splice site strengths.
GPT4All: Run Local LLMs on Any Device. Open-source and available for commercial use.
Modernity meets insane extensibility. The future of organizing your life in Neovim.
Lightning fast data version control system for large repositories of data. Feels like git, pushes and pulls like oxen.
D2 is a modern diagram scripting language that turns text to diagrams.
The fastai book, published as Jupyter Notebooks
This library provides implementations of many algorithms and data structures that are useful for bioinformatics. All provided implementations are rigorously tested via continuous integration.
Invidious is an alternative front-end to YouTube
These confs are pulled into our SWAG image: https://github.com/linuxserver/docker-swag
RNA sequencing analysis pipeline using STAR, RSEM, HISAT2 or Salmon with gene/isoform counts and extensive quality control.
ATAC-seq peak-calling and QC analysis pipeline
R package for analyzing and interactively exploring large-scale single-cell RNA-seq datasets
A repository of definition files for bootstrapping Singularity containers around the software applications, frameworks, and libraries you need to run on high-performance computing systems.
Run singularity containers on the Comet Supercomputer at San Diego Supercomputer Center
High-throughput gene to knowledge mapping through massive integration of public sequencing data.