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ShujiaHuang/README.md

Hi there, I'm Shujia Huang! 👋

Hi, I'm Shujia Huang, a bioinformatician, human genome researcher and programmer from China. My primary research interests lie in statistical modeling, bioinformatic method development and data analysis in human genetics and genomics:

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  1. BaseVar2 BaseVar2 Public

    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

    C++ 10 1

  2. mitoquest mitoquest Public

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

    C++ 6

  3. ilus ilus Public

    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…

    Python 146 36

  4. geneview geneview Public

    Genomics data visualization in Python by using matplotlib.

    Python 74 9

  5. qmplot qmplot Public

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

    Python 53 10

  6. Cpp-Primer-Plus-6th Cpp-Primer-Plus-6th Public

    《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。

    C++ 3.3k 618