plaid
PLAID computes single-sample enrichment scores for gene expression or proteomics data by calculating the average intensity of genes or proteins within gene sets.
Key Features:
- Ultra-fast computation: PLAID utilizes sparse matrix computation to achieve exceptional runtime efficiency and minimal memory requirements.
- Multi-algorithm integration: PLAID uniquely integrates the most widely used gene set scoring algorithms, enabling cross-validation with outstanding efficiency.
- Gene set score output: PLAID produces a gene set score matrix suitable for further analyses.
Scientific Applications:
- Single-cell transcriptomics: PLAID delivers highly accurate gene set scoring for single-cell gene expression profiles.
- Bulk transcriptomics: PLAID surpasses the performance of current methods for bulk RNA sequencing data.
- Proteomics: PLAID computes enrichment scores for proteomics datasets.
- Patient stratification: PLAID enables identification of unique molecular profiles to advance personalized medicine.
- Population biobanks: PLAID addresses computational inefficiencies in large-scale population datasets.
Methodology:
PLAID computes the gene set score as the average intensity of the genes or proteins in the gene set for each sample, utilizing sparse matrix computation for optimization.
Collections
Details
- License:
- GPL-3.0
- Tool Type:
- command-line tool, library
- Operating Systems:
- Linux, Mac, Windows
- Programming Languages:
- R
- Added:
- 9/1/2026
- Last Updated:
- 9/1/2026
Operations
Publications
Documentation
User manual
https://bioconductor.org/packages/plaidDownloads
- Source codehttps://bigomics.github.io/plaid/
- Source codehttps://github.com/bigomics/plaid