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.
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.· bioRxiv· 0 citations
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.
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.· bioRxiv· 0 citations
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
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· Methods in molecular biology· 0 citations
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
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