pysigscore: gene signatures scoring across bulk and single-cell transcriptomics
Giacomello, T.; Mazzara, S.; Abbruzzese, G.; Barberis, A.; tangherloni, a.; Buffa, F. M.
Show abstract
SummaryHigh-throughput transcriptomics has made gene signatures central to interpreting gene expression data, with applications in diagnosis, prognosis, and prediction. Quantifying signature activity and assessing its robustness remain challenging because scoring methods primarily rely on various assumptions, and no single approach is universally optimal. Here, we present pysigscore, a Python framework for gene set scoring in bulk and single-cell RNA-seq data. pysigscore integrates 18 built-in scoring methods with a fully customisable scorer, allowing users to define and benchmark new scoring functions. It also provides reliability analyses, including p-value estimation and leave-one-out experiments, to assess the significance of scores and gene-level contributions. We validated pysigscore on the CCLE, TCGA, and PBMC datasets, recovering the expected enrichment in liver, hypoxia, inflammatory, and cell-cycle signatures. Availability and ImplementationSource code is available at https://github.com/bioinformatics-hub/pysigscore. Contact: tommaso.giacomello@phd.unibocconi.it, francesca.buffa@unibocconi.it Supplementary informationSupplementary data are available at Bioinformatics online.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Souporcell3: Robust Demultiplexing for High-Donor Single-Cell RNA-seq Datasets 94%
- CIRCE: a scalable Python package to predict cis-regulatory DNA interactions from single-cell chromatin accessibility data 94%
- QCatch: A framework for quality control assessment and analysis of single-cell sequencing data 94%
Similar papers in this journal
Similar papers in this journal
Similar papers in this journal
Similar papers in this journal
- Single-Cell Signature Explorer for comprehensive visualization of single cell signatures across scRNA-seq data sets 95%
- CSsingle: A Unified Tool for Robust Decomposition of Bulk and Spatial Transcriptomic Data Across Diverse Single-Cell References 94%
- CorrAdjust unveils biologically relevant transcriptomic correlations by efficiently eliminating hidden confounders 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.