⚡ Clash for Lab 是为实验室环境设计的科学上网工具，无需sudo权限，优雅地一键式脚本安装

A cross-platform desktop All-in-One assistant for Claude Code, Codex, OpenCode, OpenClaw, Gemini CLI & Hermes Agent. Only official website: ccswitch.io

⭐️ A cross-platform CLI All-in-One assistant tool for Claude Code, Codex & Gemini CLI.

ARIS ⚔️ (Auto-Research-In-Sleep) — Lightweight Markdown-only skills for autonomous ML research: cross-model review loops, idea discovery, and experiment automation. No framework, no lock-in — works…

The First Innovative Tool to Comprehensively Assess T Cell States

Pleiotropy Informing Prioritisation & Evaluation (PIPE)

fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing

scooby: Modeling multi-modal genomic profiles from DNA sequence at single-cell resolution.

Single-cell copy number calling and event history reconstruction.

Single Cell Copy Number Evolutionary Analysis

Code to benchmark computational tools for estimating cell-specific copy numbers from single-cell whole-genome sequencing data.

This repository hosts the software of GEMORNA, a generative AI tool for mRNA sequence design.

上海交通大学Xflops超算队2024招新第一轮考核试题

This API provides programmatic access to the AlphaGenome model developed by Google DeepMind.

The resources of LucaOne, including: the model code, training scripts, embedding inference code, and trained checkpoints.

official repo for scPEFT

Tools for correcting single cell barcodes for various scATAC-seq techniques and creating fragment files and spltting BAM files per cluster.

This repository contains chromosome/contig name mappings between UCSC <-> Ensembl <-> Gencode for a variety of genomes.

Official code repo for the O'Reilly Book - "Hands-On Large Language Models"

Repository for the GA4GH Benchmarking Team work developing standardized benchmarking methods for germline small variant calls

processes GoT amplicon data and generates a table of metrics

In this study, we perform systematic comparative analysis of seven widely-used SNV-calling methods, including SAMtools, the GATK Best Practices pipeline, CTAT, FreeBayes, MuTect2, Strelka2 and VarS…

SCAN2 is a somatic SNV and indel genotyper for single cells amplified by Primary Template-Directed Amplification (PTA)

Formalizing and benchmarking open problems in single-cell genomics