Evidence map›Paper›PMID 42584997›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

Canon enables causal inference of downstream genes in single-cell CRISPR studies via instrumental variable analysis.

Peijun Wu, Xiang Zhou

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Peijun WuDepartment of Biostatistics, University of Michigan, Ann Arbor, MI 48109.ORCID 0000-0001-9622-8541
Xiang ZhouDepartment of Statistics and Data Science, Yale University, New Haven, CT 06511.

Funding

Statistical Methods for Modeling Polygenic Architecture in Association and Re-sequencing StudiesR01HG009124 · NHGRI · YALE UNIVERSITY · PI Xiang Zhou · 2017 to 2026
$3.0M
New directions in single cell genomics method developmentR01GM126553 · NIGMS · UNIVERSITY OF CHICAGO · PI Mengjie Chen · 2017 to 2026
$2.9M
Developing new computational tools for spatial transcriptomics dataR01HG011883 · NHGRI · UNIVERSITY OF CHICAGO · PI CHEN, MENGJIE, ZHOU, XIANG · 2021 to 2024
$1.5M
DMS/NIGMS 2: Advanced Statistical Methods for Spatially Resolved Transcriptomics StudiesR01GM144960 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHOU, XIANG · 2021 to 2024
$1.3M
HHS | NIH (NIH) R01GM126553HHS | NIH (NIH) R01GM144960HHS | NIH (NIH) R01HG009124HHS | NIH (NIH) R01HG011883NHGRI NIH HHS R01 HG009124NHGRI NIH HHS R01 HG011883NIGMS NIH HHS R01 GM126553NIGMS NIH HHS R01 GM144960
6 · The paper itself

Abstract

A critical analytical task in sc-CRISPR screening is identifying downstream genes influenced by perturbed target genes. Existing methods for this task primarily rely on traditional association-based analyses, which not only fall short in establishing causal relationships between genes but also suffer from high false positive rates and limited statistical power. To overcome these limitations, we introduce a causal inference-based framework that leverages the perturbation status of gRNAs in single cells as instrumental variables (IVs) to infer causal gene relationship via IV analysis. Building upon this framework, we further present Canon, a one-sample IV analysis method specifically tailored to systematically identify genes that are potentially causally influenced by perturbed target genes across diverse sc-CRISPR platforms. Canon ensures robust type I error control while maintaining high statistical power. We evaluated its performance through comprehensive simulations and real data applications. The gene-gene relationships identified by Canon provide valuable insights into the causal gene regulatory network, uncovering candidate therapeutic targets with potential relevance for cancer biology and demonstrating the transformative potential of sc-CRISPR screening to resolve causal regulatory networks at an unprecedented scale.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsRNA, Guide, CRISPR-Cas SystemsSingle-Cell AnalysisSoftwareComputer SimulationDatasets as TopicGene ExpressionGene Regulatory NetworksHumansLung NeoplasmsRNA, Guide, CRISPR-Cas Systemscausal relationship discoverygenomicsinstrumental variable analysissingle-cell CRISPRstatistical and computational method

Identifiers

PMID42584997
PMCPMC13486568

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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.