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Conversion between scRNA-seq objects

R 141 27 Updated Jun 21, 2024

Power calculations for Mendelian Randomisation

R 21 7 Updated Sep 27, 2017

Open-source foundation of the user-sponsored PyMOL molecular visualization system.

C 1,108 266 Updated Jul 14, 2024

Clone of the Bioconductor repository for the scRNAseq package.

R 23 12 Updated Jun 20, 2024

scINRB: single-cell gene expression imputation with network regularization and bulk RNA-seq data

R 5 Updated Jul 19, 2024
R 5 Updated Dec 23, 2023

a spatial deconvolution method based on deep learning frameworks, which converts bulk transcriptomes into spatially resolved single-cell expression profiles

Jupyter Notebook 104 22 Updated Mar 22, 2023

R/shiny interface for interactive visualization of data in SummarizedExperiment objects

R 222 43 Updated Jul 26, 2024

The bridge between the NCBI Gene Expression Omnibus and Bioconductor

R 84 36 Updated Jul 31, 2024

Access and Format Single-cell RNA-seq Datasets from Public Resources

R 28 2 Updated May 16, 2024

A LogAnalyzer app for checking logs in Posit Connect

R 6 1 Updated Jun 12, 2024

Mastering Shiny: a book

R 1,325 563 Updated Jun 20, 2024
Python 2 Updated Jul 26, 2024

SCRIP(Single Cell Regulatory network Inference using ChIP-seq) is a tool for evaluating the binding enrichment of specific TR at single-cell resolution based on scATAC-seq.

Python 18 Updated Jul 2, 2024

Cell identification in high-resolution Spatial Transcriptomics

Python 2 Updated Apr 22, 2024

STRIDE (Spatial TRanscRIptomics DEconvolution by topic modelling) is a cell-type deconvolution tool for spatial transcriptomics by using single-cell transcriptomics data.

Python 17 4 Updated Jan 23, 2024

Iso-Seq - Scalable De Novo Isoform Discovery from Single-Molecule PacBio Reads

185 61 Updated Jul 17, 2024

gwasrapidd: an R package to query, download and wrangle GWAS Catalog data

R 88 14 Updated Dec 15, 2023

Predict RNA velocity through deep learning

Jupyter Notebook 59 11 Updated Dec 12, 2023

Single-cell analysis in Python. Scales to >1M cells.

Python 1,829 591 Updated Aug 1, 2024

A tool for removing doublets from single-cell RNA-seq data

R 1 Updated Oct 30, 2023

A plugin for reading and annotating PDFs and EPUBs in obsidian.

JavaScript 1,434 63 Updated Jan 8, 2024

A deep learning-based tool to identify splice variants

Python 387 157 Updated Mar 19, 2024

Metagenomic classification of long-read sequencing data

Nextflow 46 23 Updated Jul 11, 2024
Jupyter Notebook 2 Updated May 23, 2023

This repository contains the code used in the study presented in the paper "Merging Microarray Studies and Using Random Forest to Identify a Common Gene Expression Signature in Heart Disease"

R 1 2 Updated May 29, 2020

LLM inference in C/C++

C++ 62,855 9,014 Updated Aug 1, 2024

Analysis code to reproduce all figures of "A Comprehensive Atlas of Perineuronal Net Distribution and Colocalization with Parvalbumin in the Adult Mouse Brain"

Jupyter Notebook 3 Updated Jul 14, 2023
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