Open-source Windows and Office activator featuring HWID, Ohook, TSforge, and Online KMS activation methods, along with advanced troubleshooting.

🦔 PostHog is an all-in-one developer platform for building successful products. We offer product analytics, web analytics, session replay, error tracking, feature flags, experimentation, surveys, d…

Enhanced ChatGPT Clone: Features Agents, MCP, DeepSeek, Anthropic, AWS, OpenAI, Responses API, Azure, Groq, o1, GPT-5, Mistral, OpenRouter, Vertex AI, Gemini, Artifacts, AI model switching, message…

An Open Source implementation of Notebook LM with more flexibility and features

🖥️ Run AI Agent in your browser.

User-friendly AI Interface (Supports Ollama, OpenAI API, ...)

Invoke is a leading creative engine for Stable Diffusion models, empowering professionals, artists, and enthusiasts to generate and create visual media using the latest AI-driven technologies. The …

The next version of bwa-mem

This is the official development repository for BCFtools. See installation instructions and other documentation here http://samtools.github.io/bcftools/howtos/install.html

Burrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)

Long read based human genomic structural variation detection with cuteSV

VSCode extension for code suggestion

SpecHLA reconstructs entire diploid sequences of HLA genes and infers LOH events. It supports HLA-A, -B, -C, -DPA1, -DPB1, -DQA1, -DQB1, and -DRB1 genes. Also, it supports both short- and long-read…

The sourcecode of DeepSNP

CamCNV pipeline for calling rare CNVs from Illumina data

用每个窗口的read数作为特征、胎儿浓度作为标签，训练神经网络模型；训练完成的神经网络模型可用于NIPT胎儿浓度的预测

R script for Non-invasive prenatal testing

R Package for Non Invasive Prenatal Testing (NIPT) analysis

Calling star alleles in highly polymorphic pharmacogenes (e.g. CYP450 genes) by leveraging genome graph-based variant detection.

An empirical variant annotation and data evaluation pipeline.

Frequently used commands in bioinformatics

Python for HLA analysis: summary, association analysis, zygosity test and interaction test

Bioinformatics data analysis and visualization toolkit

Evaluate variant calls and its combination with k-mer multiplicity

A high-performance, Pythonic language for bioinformatics

A GPU-friendly implementation of SpliceAI

GRIDSS: the Genomic Rearrangement IDentification Software Suite

Structural variation caller using third generation sequencing

An accurate and ultra-fast hybrid genome assembler

Long read aligner