Stars
A python library for multi omics included bulk, single cell and spatial RNA-seq analysis.
开发者边车，github打不开，github加速，git clone加速，git release下载加速，stackoverflow加速
pycaret / pycaret
8000An open-source, low-code machine learning library in Python
🚀🎉📚 APITable, an API-oriented low-code platform for building collaborative apps and better than all other Airtable open-source alternatives.
No fortress, purely open ground. OpenManus is Coming.
A mini, open-weights, version of our Proxy assistant.
PlasmidID is a mapping-based, assembly-assisted plasmid identification tool that analyzes and gives graphic solution for plasmid identification.
A feature-rich command-line audio/video downloader
使用Github Action将国外的Docker镜像转存到阿里云私有仓库，供国内服务器使用，免费易用
This is the offical codebase to reproduce and use EVOLVEpro, a model for in silico directed evolution of protein activities using few-shot active learning.
De novo clustering of long transcript reads into genes
Single-cell RNA-Seq pipeline for barcode-based protocols such as 10x, DropSeq or SmartSeq, offering a variety of aligners and empty-droplet detection
Genestrip - Efficient read classification, filtering and k-mer counting for selected groups of species
Interactive roadmaps, guides and other educational content to help developers grow in their careers.
Ultrafast consensus module for raw de novo genome assembly of long uncorrected reads. http://genome.cshlp.org/content/early/2017/01/18/gr.214270.116 Note: This was the original repository which wil…
Automatically exported from code.google.com/p/cdhit
reference-based long read assemblies of bacterial genomes
a short-read polishing tool for long-read assemblies
Tools for fast and flexible genome assembly scaffolding and improvement
为GPT/GLM等LLM大语言模型提供实用化交互接口，特别优化论文阅读/润色/写作体验，模块化设计，支持自定义快捷按钮&函数插件，支持Python和C++等项目剖析&自译解功能，PDF/LaTex论文翻译&总结功能，支持并行问询多种LLM模型，支持chatglm3等本地模型。接入通义千问, deepseekcoder, 讯飞星火, 文心一言, llama2, rwkv, claude2, m…
MiXCR is an ultimate software platform for analysis of Next-Generation Sequencing (NGS) data for immune profiling.
Copy number variant detection from targeted DNA sequencing
De novo assembler for single molecule sequencing reads using repeat graphs