zheng-xiao-sheng

zheng-xiao-sheng's Stars

• massgravel/Microsoft-Activation-Scripts

  Open-source Windows and Office activator featuring HWID, Ohook, KMS38, and Online KMS activation methods, along with advanced troubleshooting.

  Language:Batchfile95.5k9.3k

• TheGreyRaven/WinActive

  WinActive is a simple KMS Activator for Microsoft Windows/Office/VisualStudio VL Products!

  Language:C#6112

• ClementGre/ThreeFingerDragOnWindows

  Enables macOS-style three-finger dragging functionality on Windows Precision touchpads.

  Language:C#50436

• harry0703/MoneyPrinterTurbo

  利用AI大模型，一键生成高清短视频 Generate short videos with one click using AI LLM.

  Language:Python16.1k2.5k

• MRCIEU/TwoSampleMR

  R package for performing 2-sample MR using MR-Base database

  Language:R416175

• rasbt/machine-learning-notes

  Collection of useful machine learning codes and snippets (originally intended for my personal use)

  Language:Jupyter Notebook774138

• PacificBiosciences/pbbioconda

  PacBio Secondary Analysis Tools on Bioconda. Contains list of PacBio packages available via conda.

  24944

• AndreaGuarracino/1000G-ONT-F100-PGGB

  PanGenome Graph Building with the first 100 assemblies from the 1000G ONT Sequencing Consortium

  Language:R9

• bw2/SpliceAI

  A deep learning-based tool to identify splice variants

  Language:Python3

• microsoft/generative-ai-for-beginners

  18 Lessons, Get Started Building with Generative AI 🔗 https://microsoft.github.io/generative-ai-for-beginners/

  Language:Jupyter Notebook61.8k31.5k

• starskyzheng/panpop

  Application of pan-genome for population

  Language:Perl888

• kimlongli/FiveChess

  博弈能力不错的五子棋AI

  Language:C++18237

• swu1019lab/haplot

  An easy-to-use python package can be used for genomic visual analysis

  Language:Python152

• broadinstitute/sma-finder

  A tool for diagnosing SMA using exome, genome or targeted sequencing data

  Language:Python101

• gymrek-lab/LongTR

  Tandem repeat genotyping with long reads

  Language:C++20

• mills-lab/PALMER

  Pre-mAsking Long reads for Mobile Element inseRtion

  Language:C++102

• CCICB/introme

  Introme prioritises coding and noncoding splice-altering variants for clinical variant interpretation

  Language:Shell193

• PacificBiosciences/trgt

  Tandem repeat genotyping and visualization from PacBio HiFi data

  Language:Rust997

• lh3/srf

  SRF: Satellite Repeat Finder

  Language:TeX826

• Jong-hun-Park/trviz

  A python library for decomposing and visualizing tandem repeat sequences

  Language:Python9

• google/deepvariant

  DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.

  Language:Python3.2k713

• gagneurlab/absplice

  Language:Python334

• gagneurlab/splicemap

  Language:Jupyter Notebook184

• shohei-kojima/MEGAnE

  MEGAnE

  Language:Python242

• clemgoub/rm2gff3

  Convert RepeatMasker ".out" file into a gff3 with colors!!!

  Language:Shell192

• ZhouYing0818/Entropy_Weight_Ensemble

  Language:R2

• bio-ontology-research-group/phenomenet-vp

  A phenotype-based tool for variant prioritization in WES and WGS data

  Language:Java3613

• bzhanglab/GISTIC2_example

  a example script and reference files to run GISTIC2

  Language:Shell73

• JohannKaspar/AutoCaSc

  AutoCaSc is a tool for evaluating deleteriousness of genomic variants found in Trio Exome Sequencing in cases of neurodevelopmental disorders (NDD).

  Language:Python91

• broadinstitute/seqr

  web-based analysis tool for rare disease genomics

  Language:Python17688