Jun Zhang's starred repositories
bam-readcount
Count bases in BAM/CRAM files
VcfHunter
VcfExplorer regroups several programs which principal aims are to map DNA and RNAseq data onto reference genome sequence, perform variant calling, manipulate vcf files, perform chromosome painting of accessions based on the contribution of ancestral groups, select marker for genetic map analysis and perform pairwise chromosome linkage of ordered markers.
RNA-seq-analysis
RNAseq analysis notes from Ming Tang
research-method
论文写作与资料分享
UnderstandingDeepLearning-ZH-CN
UnderstandingDeepLearing中文翻译
BAMixChecker
BAMixChecker: A fast and efficient tool for sample matching checkup
annotated_deep_learning_paper_implementations
🧑🏫 60+ Implementations/tutorials of deep learning papers with side-by-side notes 📝; including transformers (original, xl, switch, feedback, vit, ...), optimizers (adam, adabelief, sophia, ...), gans(cyclegan, stylegan2, ...), 🎮 reinforcement learning (ppo, dqn), capsnet, distillation, ... 🧠
Heritability
Heritability in plant breeding - R and SAS code examples
hello-algo
《Hello 算法》:动画图解、一键运行的数据结构与算法教程。支持 Python, Java, C++, C, C#, JS, Go, Swift, Rust, Ruby, Kotlin, TS, Dart 代码。简体版和繁体版同步更新,English version ongoing
vgp-assembly
VGP repository for the genome assembly working group
subgenome_phasing_example
An Example of Subgenome Phasing for Complex Allopolyploidy
AlleleSorting
R scripts for automated identification of parental homeologs and subsequent sorting of alleles.
telomeric-identifier
Identify and find telomeres, or telomeric repeats in a genome.
Centromics
Centromics: visualing centromeres with multiple omics data