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Visualization of scRNA-seq data.

HTML 93 19 Updated Nov 10, 2022

Conversion between scRNA-seq objects

R 144 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 1,133 271 Updated Sep 5, 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 7 Updated Jul 19, 2024
R 6 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 108 23 Updated Mar 22, 2023

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

R 222 42 Updated Sep 3, 2024

The bridge between the NCBI Gene Expression Omnibus and Bioconductor

R 87 36 Updated Aug 6, 2024

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

R 29 3 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 1,334 564 Updated Jun 20, 2024
Python 3 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

186 61 Updated Jul 17, 2024

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

R 89 15 Updated Dec 15, 2023

Predict RNA velocity through deep learning

Jupyter Notebook 60 11 Updated Dec 12, 2023

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

Python 1,863 595 Updated Sep 5, 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 1,461 68 Updated Jan 8, 2024

A deep learning-based tool to identify splice variants

Python 397 156 Updated Mar 19, 2024

Metagenomic classification of long-read sequencing data

Nextflow 51 23 Updated Sep 6, 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++ 64,606 9,247 Updated Sep 7, 2024
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