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Cpp-Primer-Plus-6th
《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。ilus
A handy variant calling pipeline generator for whole-genome sequencing (WGS) and whole exom sequencing data (WES) analysis. 一个简易且全面的 WGS/WES 分析流程生成器.geneview
Genomics data visualization in Python by using matplotlib.qmplot
A Python package for creating high-quality manhattan and Q-Q plots from GWAS results.cmdbtools
Command line tools for CMDB varaints browserbasevar
This is the official development repository for BaseVar, which call variants for large-scale ultra low-pass (<1.0x) WGS data, especially for NIPT datadraw_ngs
Programs for drawing chromosome figure by using NGS databioweekly
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。genedev-introduce
基因组学挑战题说明RefHap
A Reliable and Fast Algorithm for Single Individual Haplotypinghuangshujia.com
A personal website for Shujia HuangShujiaHuang.github.io
GitHub homepage of huangshujia.meAsmVar2
【Force on Genotyping】A new and practical human (or diploid) genome variants caller for de novo assembly or long reads alignmentSOAPaligner
SOAPaligner(also named soap2) is a member of the SOAP (Short Oligonucleotide Analysis Package). It is an updated version of SOAP software for short oligonucleotide alignment.speedwgs
MachineLearning_Note
Notes for machine learningngslib
A C++ library for reading high-throughput sequencing data.gatk_pipeline
GATK Pipeline: Recalibrates mapping qualities and calls variants using GATKLove Open Source and this site? Check out how you can help us