Bulk RNA-seq deconvolution with Bulk2Single

Community

Deconvolute bulk RNA-seq to single-cell.

AuthorStarlitnightly
Version1.0.0
Installs0

System Documentation

What problem does it solves? Extracting single-cell resolution information from bulk RNA-seq data is a key challenge in genomics. This Skill automates the deconvolution process, generating synthetic single-cell profiles and benchmarking them against reference atlases to provide deeper insights.

Core Features & Use Cases

  • Cell Fraction Estimation: Accurately estimate cell-type fractions from bulk RNA-seq using integrated TAPE estimators.
  • Synthetic Cell Generation: Generate high-quality synthetic single-cell datasets using a beta-VAE model.
  • Quality Control & Benchmarking: Filter generated cells and benchmark their cluster proportions and correlations against reference scRNA-seq data.
  • Use Case: Transform bulk tumor RNA-seq data into synthetic single-cell profiles, estimate the proportions of different immune and tumor cell types, and then compare these generated cells to a known single-cell atlas for validation.

Quick Start

Deconvolute my bulk RNA-seq data into synthetic single cells using Bulk2Single, then estimate cell fractions and compare generated cells to a reference atlas.

Dependency Matrix

Required Modules

omicversescanpyscveloanndatamatplotlibnumpypandastorch

Components

references

💻 Claude Code Installation

Recommended: Let Claude install automatically. Simply copy and paste the text below to Claude Code.

Please help me install this Skill:
Name: Bulk RNA-seq deconvolution with Bulk2Single
Download link: https://github.com/Starlitnightly/omicverse/archive/main.zip#bulk-rna-seq-deconvolution-with-bulk2single

Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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