raksasa's Stars
yescallop/areacodes
中华人民共和国县级以上历史行政区划代码及新旧代码对应关系数据集
ai-collection/ai-collection
The Generative AI Landscape - A Collection of Awesome Generative AI Applications
awesomedata/awesome-public-datasets
A topic-centric list of HQ open datasets.
binary-husky/gpt_academic
为GPT/GLM等LLM大语言模型提供实用化交互接口,特别优化论文阅读/润色/写作体验,模块化设计,支持自定义快捷按钮&函数插件,支持Python和C++等项目剖析&自译解功能,PDF/LaTex论文翻译&总结功能,支持并行问询多种LLM模型,支持chatglm3等本地模型。接入通义千问, deepseekcoder, 讯飞星火, 文心一言, llama2, rwkv, claude2, moss等。
SuperCV/Book
:green_book:我的个人书籍学习和收藏
anzhihe/learning
Learning Shell,Python,Golang,System,Network
liyu95/Deep_learning_examples
Examples of using deep learning in Bioinformatics
ga4gh/vrs-python
GA4GH Variation Representation Python Implementation
ohmeta/metapi
A general metagenomics data mining system focus on robust microbiome research
NCBI-Hackathons/TheHumanPangenome
A Strategy for Building and Using a Human Reference Pangenome
Pfern/PANGenomics
popgenmethods/lecture_notes
Lecture Notes on Computational and Mathematical Population Genetics
AurelWu/HexMapLibrary
working with hexagonal maps in unity made easy.
cloudhu/HexMapMadeInUnity2019ECS
Auto Create Map System Made with Unity 2019 ECS
vgteam/graph-genomics-review
Pangenome graphs (review article on graph-based pangenomic methods)
Martiantian/Somatic_cnv_detect_tool
cfDNA sequencing cnv analyze pipeline
OpenGene/ctdna-pipeline
A simplified pipeline for ctDNA sequencing data analysis
chenyu600/rdscreening
nanoporetech/pipeline-structural-variation
Pipeline for calling structural variations in whole genomes sequencing Oxford Nanopore data
deaconjs/ThousandVariantCallersRepo
Thousand Variant Callers Project Repository
tobiasrausch/alfred
BAM Statistics, Feature Counting and Annotation
PacificBiosciences/sv-benchmark
Public Benchmark of Long-Read Structural Variant Caller on PacBio CCS HG002 Data
MGI-tech-bioinformatics/MGI_DeepVariant_model
MGI train model
rrwick/Long-read-assembler-comparison
Benchmarking of long-read assembly tools for bacterial whole genomes
lh3/seqtk
Toolkit for processing sequences in FASTA/Q formats
livnatje/ImmuneResistance
This resource provides the code developed in the study of Jerby-Arnon _et al. "Single-cell RNA-seq of melanoma ecosystems reveals sources of T cell exclusion linked to immunotherapy clinical outcomes".
gpakosz/.tmux
🇫🇷 Oh my tmux! My self-contained, pretty & versatile tmux configuration made with ❤️
google/deepvariant
DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
sterding/BRAINcode
Script and pipeline for BRAINcode project
CCDG/Pipeline-Standardization