Evidence map›Paper›PMID 39779958›Full record

ArticleNature genetics2025

Transcript-specific enrichment enables profiling of rare cell states via single-cell RNA sequencing.

Tsion Abay, Robert R Stickels, Meril T Takizawa, Benan N Nalbant, Yu-Hsin Hsieh, Sidney Hwang, Catherine Snopkowski, Kenny Kwok Hei Yu, Zaki Abou-Mrad, Viviane Tabar and 5 more

Abstract read
In one paragraph

Article in Nature genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
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  6. Review
  7. Genome-wide single-cell perturbation screens with VIPerturb-seq.bioRxiv : the preprint server for biology · 2026
    Article
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  10. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Tsion Abay *Department of Pathology, Stanford University, Stanford, CA, USA.
Robert R Stickels *Department of Pathology, Stanford University, Stanford, CA, USA. rstickel@stanford.edu.ORCID http://orcid.org/0000-0003-4326-4084
Meril T Takizawa *Single-cell Analytics Innovation Lab, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Benan N NalbantComputational and Systems Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Yu-Hsin HsiehComputational and Systems Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Sidney HwangDepartment of Pathology, Stanford University, Stanford, CA, USA.
Catherine SnopkowskiSingle-cell Analytics Innovation Lab, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Kenny Kwok Hei YuDepartment of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-2394-4990
Zaki Abou-MradDepartment of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0001-6387-8396
Viviane TabarDepartment of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-1284-1670
Brooke E HowittDepartment of Pathology, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-0309-6680
Leif S LudwigBerlin Institute of Health at Charité-Universitätsmedizin Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0002-2916-2164
Ronan ChalignéSingle-cell Analytics Innovation Lab, Memorial Sloan Kettering Cancer Center, New York, NY, USA. chalignr@mskcc.org.ORCID http://orcid.org/0000-0003-4332-3291
Ansuman T SatpathyDepartment of Pathology, Stanford University, Stanford, CA, USA. satpathy@stanford.edu.ORCID http://orcid.org/0000-0002-5167-537X
Caleb A LareauComputational and Systems Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA. lareauc@mskcc.org.ORCID http://orcid.org/0000-0003-4179-4807

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Single-cell Mapping Center for Human Regulatory Elements and Gene ActivityUM1HG012076 · NHGRI · STANFORD UNIVERSITY · PI Michael Ryan Corces, Ansuman Satpathy · 2021 to 2026
$13.8M
The Human DNA virome: from petabase scale to single-cell resolutionU01AT012984 · NCCIH · SLOAN-KETTERING INST CAN RESEARCH · PI Caleb Andrew Lareau · 2024 to 2026
$5.2M
Charting somatic evolution via single-cell multiomicsR00HG012579 · NHGRI · SLOAN-KETTERING INST CAN RESEARCH · PI LAREAU, CALEB ANDREW · 2023 to 2025
$747k
NCCIH NIH HHS U01 AT012984NCI NIH HHS P30 CA008748NHGRI NIH HHS R00 HG012579NHGRI NIH HHS UM1 HG012076U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P30CA008748U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) R00HG012579U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) UM1HG012076
6 · The paper itself

Abstract

Single-cell genomics technologies have accelerated our understanding of cell-state heterogeneity in diverse contexts. Although single-cell RNA sequencing identifies rare populations that express specific marker transcript combinations, traditional flow sorting requires cell surface markers with high-fidelity antibodies, limiting our ability to interrogate these populations. In addition, many single-cell studies require the isolation of nuclei from tissue, eliminating the ability to enrich learned rare cell states based on extranuclear protein markers. In the present report, we addressed these limitations by developing Programmable Enrichment via RNA FlowFISH by sequencing (PERFF-seq), a scalable assay that enables scRNA-seq profiling of subpopulations defined by the abundance of specific RNA transcripts. Across immune populations (n = 184,126 cells) and fresh-frozen and formalin-fixed, paraffin-embedded brain tissue (n = 33,145 nuclei), we demonstrated that programmable sorting logic via RNA-based cytometry can isolate rare cell populations and uncover phenotypic heterogeneity via downstream, high-throughput, single-cell genomics analyses.

Indexed as

Gene Expression ProfilingSequence Analysis, RNASingle-Cell AnalysisAnimalsBrainFlow CytometryHumansMiceRNA-Seq

Identifiers

PMID39779958
PMCPMC12276987

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.