Skip to content
Open access

Joint analysis of multiply perturbed cells improves statistical power and cost efficiency in Perturb-seq

Jul 2026 · bioRxiv · 0 citations · 45 references
Biology

TL;DR

Overall, this work recommends a design that intentionally includes single-guide cells, guide doublets, and guide triplets to improve cost efficiency while preserving signal recovery, and develops PerturbMatch, a scalable statistical framework to analyze guide multiplets.

Abstract

Perturb-seq measures transcriptomic responses to genetic perturbations at scale, but conventional designs that enrich for one guide RNA per cell remain resource-intensive. Standard analyses discard cells carrying multiple guides, further limiting the usable yield from each experiment. Here, we characterize how incorporating these guide multiplets affects signal recovery, information loss, and cost reduction. At the highest guide burden, cells showed increased stress and suppressed cell-cycle progression. We develop PerturbMatch, a scalable statistical framework to analyze guide multiplets. Among different classes of guide multiplets, doublets and triplets recovered perturbation responses more accurately than higher-order multiplets. Across three 5000-gene Perturb-seq screens with increasing guide loading, per-cell costs decreased by up to 81% while information loss remained within 1.5-fold of the loss observed between technical replicates. In existing genome-wide Perturb-seq data, incorporating previously discarded guide multiplets increased usable cell numbers and improved statistical power. Compared with a singlet holdout set, adding guide multiplets moved signal recovery closer to the theoretical expected reproducibility. Overall, we recommend a design that intentionally includes single-guide cells, guide doublets, and guide triplets to improve cost efficiency while preserving signal recovery.

Read PDF

Similar papers

Open access Aug 2026

Perturb-ME: Scalable mechanism discovery from phenotype-enriched genome-wide screens

Perturb-ME, along with agentic interpretation, provide a scalable framework for comprehensive functional discovery from phenotype-enriched genetic screens and combines genome-scale CRISPR screening, phenotype-based enrichment and multimodal single-cell profiling.

Han-Chen Wang, Jiacheng Gu, Chris J. Frangieh et al. · 0 citations
Open access Aug 2026

Characterizing and mitigating cross-library PCR chimeras in Perturb-seq using Perturb-Audit

Perturb-Audit, a diagnostic and denoising framework that integrates molecule-level collision auditing with statistical background suppression, supports an audit-first strategy to improve assignment fidelity and biological interpretability in single-cell CRISPR screens.

Xin Song, Jiayi Lu, Ping Zhu · 0 citations
Open access Aug 2026

Reliable single-cell perturbations explain and improve model performance

This work tests the reliability of perturbations and their alignment with shared perturbation responses, classifying each perturbation as specific, shared, or unreliable, and applies these quality labels to published benchmarks shows that model comparisons depend on perturbation quality.

Xi Wang, J. Kuipers, Florian Hugi et al. · 0 citations
#artificial intelligence Preprint Sep 2026

PopPert: Population-level Joint-Distribution Modeling for Single-Cell Perturbation Prediction

PopPert predicts perturbation-induced changes in distribution parameters, eliminating the need for cell-level correspondence and reducing sensitivity to single-cell noise, establishing population-level joint distribution learning as an effective paradigm for predicting transcriptional responses from unpaired single-cel...

Han-Dong Wang, Jiaxin Qi, Hao-Chen Feng et al. · 0 citations
2026

Comprehensive Guide to Gene Expression Analysis from Bulk and Single-Nucleus Transcriptomes.

This chapter covers quality control, normalization, sparse data handling, and transcript quantification for both bulk and snRNA-seq, along with strategies to address challenges such as multi-mapped reads and batch effects, and examines how artificial intelligence and machine learning techniques can improve data process...

S. P. Dharshini, Y.-H. Taguchi, M. Gromiha · 0 citations
#artificial intelligence Preprint Sep 2026

AmbiModBench: Benchmarking Gene Perturbation Prediction Beyond Shared Responses

Predicting cellular responses to genetic perturbations helps prioritize experiments in single-cell genomics, where exhaustive measurement is infeasible. While computational models increasingly predict these responses, three evaluation deficiencies obscure what their scores demonstrate. First, absolute metrics cannot se...

Si-Kai Huang, Zhi-Wen Yang, Kai Yu et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.