wangpanqiao

ohmyzsh

🙃 A delightful community-driven (with 2,300+ contributors) framework for managing your zsh configuration. Includes 300+ optional plugins (rails, git, macOS, hub, docker, homebrew, node, php, python, etc), 140+ themes to spice up your morning, and an auto-update tool so that makes it easy to keep up with the latest updates from the community.

jupyterlab

JupyterLab computational environment.

docker-stacks

Ready-to-run Docker images containing Jupyter applications

clashfree

clash节点、免费clash节点、免费节点、免费梯子、clash科学上网、clash翻墙、clash订阅链接、clash for Windows、clash教程、免费公益节点、最新clash免费节点订阅地址、clash免费节点每日更新

techxuexi-js

油猴等插件的 学习强国 js 代码 45分/天

Moss

Moss(莫斯)-Spring Cloud体系的服务治理平台，让Spring Cloud应用不再流浪！欢迎Star！

tableExport.jquery.plugin

"table2JSON", "table2XML", "table2PNG","table2CSV","table2Excel","table2Word","table2Powerpoint","table2txt","table2PDF"

xxqg

学习强国 xxqg 无人值守自动看视频、看文章、自动答题（每日答题、每周答题、专项答题），45分/天

Learn-Bioinformatics-by-RNA-seq

Biostat-578

A repository for all of my teaching material

bioinformatics123

NGSCheckMate

Software program for checking sample matching for NGS data

CAFE5

Version 5 of the CAFE phylogenetics software

transanno

accurate LiftOver tool for new genome assemblies

tech-study-node

基于Node.js的自动化学习强国工具 40分/天 A tools helps you with xuexiqiangguo based on Node.js.

DNNGP

DNNGP: Deep neural network for genomic prediction

GWAS-pipeline

This is a general (somewhat comprehensive) description of the LNG GWAS pipeline which can be used to guide researchers on how-to run a GWAS.

vcf2fasta

Converts a VCF file to a FASTA alignment provided a reference genome and a GFF file

molgenis-pipelines

Pipelines for NGS, imputation, gwas, ...

rnaseq_tutorial_wiki

The wiki repo, with pull request enabled, for the rnaseq_tutorial

GeneDoc

A Full Featured Multiple Sequence Alignment Editor.

bsa

Bulked-Segregant Analysis using vcf file with or without parents

Biochem-3BP3

Lectures and Lab Exercises for Biochem 3BP3 Practical Bioinformatics for the Genomics Era

learning-RNA-Seq

bioinformatics

tools for biolinux

vcf2fasta

reference fasta to diploid fasta via SNPs in VCF

vcf2geno

Efficiently Read Variant Call Format (VCF) into R

scripts

scripts

dQTG.seq

:exclamation: This is a read-only mirror of the CRAN R package repository. dQTG.seq — A BSA Software for Detecting All Types of QTLs in BC, DH, RIL and F2

VCF2Genomes_python_Codes