adamewing's Stars
jmorganca/ollama
Get up and running with Llama 2, Mistral, and other large language models locally.
pola-rs/polars
Dataframes powered by a multithreaded, vectorized query engine, written in Rust
Textualize/textual
The lean application framework for Python. Build sophisticated user interfaces with a simple Python API. Run your apps in the terminal and a web browser.
tloen/alpaca-lora
Instruct-tune LLaMA on consumer hardware
reflex-dev/reflex
🕸️ Web apps in pure Python 🐍
exaloop/codon
A high-performance, zero-overhead, extensible Python compiler using LLVM
paul-gauthier/aider
aider is AI pair programming in your terminal
togethercomputer/RedPajama-Data
The RedPajama-Data repository contains code for preparing large datasets for training large language models.
red-data-tools/YouPlot
A command line tool that draw plots on the terminal.
jmschrei/pomegranate
Fast, flexible and easy to use probabilistic modelling in Python.
jaymody/picoGPT
An unnecessarily tiny implementation of GPT-2 in NumPy.
npiv/chatblade
A CLI Swiss Army Knife for ChatGPT
piccolomo/plotext
plotting on terminal
jokergoo/ComplexHeatmap
Make Complex Heatmaps
bloomberg/pystack
🔍 🐍 Like pstack but for Python!
bugen/pypipe
Python pipe command line tool
deeptools/pyGenomeTracks
python module to plot beautiful and highly customizable genome browser tracks
amaiya/onprem
A tool for running on-premises large language models with non-public data
ComparativeGenomicsToolkit/cactus
Official home of genome aligner based upon notion of Cactus graphs
kbressem/medAlpaca
LLM finetuned for medical question answering
igvteam/igv-reports
Python application to generate self-contained pages embedding IGV visualizations, with no dependency on original input files.
brentp/goleft
goleft is a collection of bioinformatics tools distributed under MIT license in a single static binary
hartwigmedical/hmftools
Various algorithms for analysing genomics data
statgen/locuszoom
A Javascript/d3 embeddable plugin for interactively visualizing statistical genetic data from customizable sources.
KolmogorovLab/Severus
A tool for somatic structural variant calling using long reads
HKU-BAL/ClairS
ClairS - a deep-learning method for long-read somatic small variant calling
Xinglab/espresso
fritzsedlazeck/Spectre
Copy number caller for long read data including SNV utilization
FenyoLab/L1EM
Estimate locus specific human LINE-1 expression.
wdecoster/kyber