Evidence map›Paper›PMID 42241464›Full record

ArticlePLoS computational biology2026

CIPHER: An end-to-end framework for designing optimized aggregated spatial transcriptomics experiments.

Zachary Hemminger, Haley De Ocampo, Fangming Xie, Zhiqian Zhai, Jingyi Jessica Li, Roy Wollman

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Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Zachary HemmingerDepartment of Chemistry and Biochemistry, University of California, Los Angeles, California, United States of America.
Haley De OcampoDepartment of Chemistry and Biochemistry, University of California, Los Angeles, California, United States of America.
Fangming XieDepartment of Chemical Biology, David Geffen School of Medicine, University of California, Los Angeles, California, United States of America.ORCID 0000-0001-5232-1648
Zhiqian ZhaiDepartment of Statistics and Data Science, University of California, Los Angeles, California, United States of America.ORCID 0009-0001-3104-7472
Jingyi Jessica LiDepartment of Statistics and Data Science, University of California, Los Angeles, California, United States of America.
Roy WollmanDepartment of Chemistry and Biochemistry, University of California, Los Angeles, California, United States of America.ORCID 0000-0003-3865-2605

Funding

Whole organ transcriptome reconstruction by dimensionality reduced fluorescent in situ hybridizationR01HG012925 · NHGRI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Jingyi Jessica Li, Roy Wollman · 2024 to 2026
$1.9M
NHGRI NIH HHS R01 HG012925NIH HHS R01-HG012925
6 · The paper itself

Abstract

motivationMost imaging-based spatial transcriptomics methods measure individual genes, which limits scalability and typically requires integration with scRNA-seq to recover full cellular states. Recent approaches such as CISI, FISHnCHIPs, and ATLAS address this limitation by measuring aggregate transcriptional signatures, where multiple genes are pooled into each channel to increase throughput. While aggregate measurements improve scalability, they shift the problem from gene selection to feature design. For effective integration with scRNA-seq, these signatures must be not only discriminative in transcriptional space but also straightforward to measure, with balanced signal, sufficient dynamic range, and robustness to experimental noise. By optimizing decoding accuracy in isolation, existing methods leave substantial performance on the table.

resultsWe present CIPHER (Cell Identity Projection using Hybridization Encoding Rules), a neural-network framework that jointly optimizes the experimental encoding matrix, i.e., the way that genes are aggregated to signatures, and the downstream cell embedding. CIPHER integrates the physical limits of imaging assays directly into its loss function, shaping the latent space to maximize discriminability while maintaining robustness to measurement noise and signal constraints. Using a large-scale mouse brain scRNA-seq reference, we show that CIPHER-designed encodings yield latent spaces with improved cell-type separability, uniform signal utilization, and greater resilience to hybridization variability, resulting in higher decoding accuracy from both simulated and experimental data.

conclusionCIPHER formulates aggregate signature design as a joint optimization problem over decoding accuracy and experimental measurability. This enables systematic, scRNA-seq-aligned feature design for scalable spatial transcriptomics based on aggregate measurements. AVAILABILITY: Code and documentation are available at https://github.com/wollmanlab/Design/.

Indexed as

Spatial TranscriptomicsAlgorithmsAnimalsComputational BiologyMiceSingle-Cell Gene Expression AnalysisSoftwareTranscriptome

Identifiers

PMID42241464
PMCPMC13252831

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.