《C++ Primer Plus 第6版（中文版）》原书代码、习题答案和个人笔记，仅供学习和交流。

fastlckin: A high-performance C++17 tool for maximum likelihood kinship estimation from low-coverage sequencing data using genotype likelihoods.

This is the official development repository for BaseVar, which call variants for large-scale ultra low-depth(<1.0x) WGS data, especially for NIPT data and ancient DNA

Human Mitochondrial sequencing data Analysis Toolkit. Fetching information like variants, heteroplasmy/homoplasmy, etc. on mitochondrial genome from sequencing data

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

ASCII generator (image to text, image to image, video to video)

《大语言模型》作者：赵鑫，李军毅，周昆，唐天一，文继荣

A NGS data analysis toolkit

A phasing and imputation pipeline for NGS data

Dear ImGui: Bloat-free Graphical User interface for C++ with minimal dependencies

software tools for haplotype assembly from sequence data

Methylation/modified base calling separated from basecalling.

A community-maintained Python framework for creating mathematical animations.

Animation engine for explanatory math videos

C 语言教程

GDBIGtools: A command line tools for GDBIG varaints browser

C++ 资源大全中文版，标准库、Web应用框架、人工智能、数据库、图片处理、机器学习、日志、代码分析等。由「开源前哨」和「CPP开发者」微信公号团队维护更新。

A library of free open source icons for science illustrations in biology and chemistry

Rsync GitHub Action

GitHub Actions for executing remote ssh commands.

这里记录每周值得分享的生命科学和生物信息学进展内容，周日发布。

中文技术文档的写作规范

Clairvoyante: a multi-task convolutional deep neural network for variant calling in Single Molecule Sequencing

A Python package for creating high-quality manhattan and Q-Q plots from GWAS results.

A lightweight and handy variant calling pipeline generator for whole-genome sequencing (WGS) and whole exom sequencing data (WES) analysis by using GATK and Sentieon. 一个基于 GATK 和 Sentieon 的简易且全面的 W…

Programs for drawing chromosome figure by using NGS data

Official code repository for GATK versions 4 and up

A Reliable and Fast Algorithm for Single Individual Haplotyping

This is the official development repository for BaseVar, which call variants for large-scale ultra low-pass (<1.0x) WGS data, especially for NIPT data

Command line tools for CMDB varaints browser