Evidence map›Paper›PMID 40790054›Full record

ArticleScientific reports2025

Miniaturized scalable arrayed CRISPR screening in primary cells enables discovery at the single donor resolution.

Miti A Patel, Brittany P Boribong, Hugo Sinha, Bin Xiao, Keqiang Xie, Philippe Q N Vo, Andrew B Chin, Ayoub Ellouzi, Samuel R Little, Steve C C Shih and 3 more

Erratum issuedAbstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Miti A Patel *DropGenie, Cambridge, MA, USA.
Brittany P Boribong *DropGenie, Cambridge, MA, USA.
Hugo SinhaDropGenie, Cambridge, MA, USA.
Bin XiaoDepartment of Biochemistry, McGill University, Montreal, Canada.
Keqiang XieFull Circles Therapeutics, Cambridge, MA, USA.
Philippe Q N VoDropGenie, Cambridge, MA, USA.
Andrew B ChinDropGenie, Cambridge, MA, USA.
Ayoub EllouziDropGenie, Cambridge, MA, USA.
Samuel R LittleDepartment of Electrical and Computer Engineering, Concordia University, Montréal, QC, Canada.
Steve C C ShihDepartment of Electrical and Computer Engineering, Concordia University, Montréal, QC, Canada.
Hao WuFull Circles Therapeutics, Cambridge, MA, USA.
William J MullerDepartment of Biochemistry, McGill University, Montreal, Canada.
Alison HirukawaDropGenie, Cambridge, MA, USA. alison@drop-genie.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-efficiency gene editing in primary human cells is critical for advancing therapeutic development and functional genomics, yet conventional electroporation platforms often require high cell input and are poorly suited to parallelized experiments. Here we introduce a next-generation digital microfluidics (DMF) electroporation platform that enables high-throughput, low-input genome engineering using discrete droplets manipulated on a planar electrode array. The system supports 48 independently programmable reaction sites and integrates seamlessly with laboratory automation, allowing efficient delivery of CRISPR-Cas9 RNPs and mRNA cargo into as few as 3,000 primary human cells per condition. The platform was validated across diverse primary human cell types and cargo modalities, demonstrating efficient delivery of various cargo, with high rates of transfection, gene knockout via non-homologous end joining, and precise knock-in through homology-directed repair. To showcase its utility in functional genomics, we applied the platform to an arrayed CRISPR-Cas9 screen in chronically stimulated human CD4⁺ T cells, identifying novel regulators of exhaustion, including epigenetic and transcriptional modulators. These findings establish our DMF-based electroporation platform as a powerful tool for miniaturized genome engineering in rare or precious cell populations and provide a scalable framework for high-content genetic screening in primary human cells.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsGene EditingCD4-Positive T-LymphocytesElectroporationHumansMicrofluidicsMiniaturization

Identifiers

PMID40790054
PMCPMC12339676

What OpenQuestion holds

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Registered trials

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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.