Evidence map›Paper›PMID 41889931›Full record

ArticlebioRxiv : the preprint server for biology2026

pertTF: context-aware AI modeling for genome-scale and cross-system perturbation prediction.

Yangqi Su, Dingyu Liu, Vipin Menon, Bicna Song, Samuel Boccara, Nan Zhang, Huan Zhao, Jiahui Hazel Zhao, Lei Wang, Nan Hu and 10 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for 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.

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

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Yangqi SuUniversity of Maryland-Institute for Health Computing, North Bethesda MD 20852.
Dingyu LiuDevelopmental Biology Program, Sloan Kettering Institute; 1275 York Avenue, New York, NY 10065, USA.
Vipin MenonUniversity of Maryland-Institute for Health Computing, North Bethesda MD 20852.
Bicna SongCenter for Cancer and Immunology Research, Children's National Hospital, 111 Michigan Ave NW, Washington, DC 20010, USA.
Samuel BoccaraDepartment of Computer Science, University of Maryland College Park, College Park MD 20742.
Nan ZhangDevelopmental Biology Program, Sloan Kettering Institute; 1275 York Avenue, New York, NY 10065, USA.
Huan ZhaoCecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Jiahui Hazel ZhaoDevelopmental Biology Program, Sloan Kettering Institute; 1275 York Avenue, New York, NY 10065, USA.
Lei WangCecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Nan HuDevelopmental Biology Program, Sloan Kettering Institute; 1275 York Avenue, New York, NY 10065, USA.
Mpathi NzimaCecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Alon KatzUniversity of Maryland-Institute for Health Computing, North Bethesda MD 20852.
Bharath Kumar SwargamInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore MD 21201.
Seth A AmentInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore MD 21201.
Yarui DiaoDepartment of Cell Biology, Duke University Medical Center, Durham, NC, USA.
Hanrui ZhangCardiometabolic Genomics Program, Department of Medicine - Cardiology, Columbia University Irving Medical Center, New York, NY 10032.
Lumen ChaoCenter for Precision Medicine and Genomics Research, Children's National Hospital. 111 Michigan Ave NW, Washington, DC 20010, USA.
Gary HonCecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Danwei HuangfuDevelopmental Biology Program, Sloan Kettering Institute; 1275 York Avenue, New York, NY 10065, USA.
Wei LiUniversity of Maryland-Institute for Health Computing, North Bethesda MD 20852.ORCID 0000-0002-2163-7903

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
UNIVERSITY OF MARYLAND GREENEBAUM CANCER CENTERSUPPORT GRANTP30CA134274 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI FEYRUZ VIRGILIA RASSOOL · 2008 to 2026
$51.0M
Center for scalable knockout and multimodal phenotyping in genetically diverse human genomesUM1HG012654 · NHGRI · SLOAN-KETTERING INST CAN RESEARCH · PI Danwei Huangfu, LORENZ P. STUDER · 2022 to 2026
$9.1M
Genomic control of gene regulatory networks governing early human lineagedecisionsU01HG012051 · NHGRI · SLOAN-KETTERING INST CAN RESEARCH · PI Michael A Beer, ANNA-KATERINA HADJANTONAKIS · 2021 to 2026
$8.3M
Regulation of DNA methylation by TETs and QSER1R01HD111256 · NICHD · WEILL MEDICAL COLL OF CORNELL UNIV · PI Todd R Evans, Danwei Huangfu · 2022 to 2026
$3.4M
Integrative genomic and functional genomic studies to connect variant to function for CAD GWAS lociR01HL168174 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Wei Li, EDOARDO MARCORA · 2023 to 2026
$3.1M
Modeling Heterogenous Outcomes in Functional Genetic Screens Using Single-cell Genomics as ReadoutsR01HG010753 · NHGRI · CHILDREN'S RESEARCH INSTITUTE · PI LI, WEI · 2019 to 2023
$2.5M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA134274NHGRI NIH HHS R01 HG010753NHGRI NIH HHS U01 HG012051NHGRI NIH HHS UM1 HG012654NHLBI NIH HHS R01 HL168174NICHD NIH HHS R01 HD111256
6 · The paper itself

Abstract

Predicting genetic perturbation responses at a single-cell level is central to building models for cell state and disease. However, existing approaches are limited on predicting phenotypic outcomes beyond expression changes and generalizing predictions across genome-scale perturbations in biologically relevant contexts. Here we introduce pertTF, a transformer-based single-cell genetic perturbation model. pertTF was trained from a unique dataset capturing single cell expressions profiles of 30 full gene knockouts across 14 relevant cell types during human pancreatic development and beta-cell differentiation. pertTF outperforms current methods in predicting expression changes of perturbing unseen genes in unseen cellular contexts. In addition, pertTF infers perturbation-induced shifts in cell identity and population composition, an important phenotypic outcome of perturbation in many physiology and disease settings. Through transfer learning, pertTF operates in physiologically relevant systems, including primary human islets, where large-scale perturbation experiments are challenging. The generalizability of pertTF is further demonstrated by in silico pooled and single-cell CRISPR screens, capturing critical regulators of stem cells and early pancreatic cell development. These results establish pertTF as a framework for integrating large-scale single-cell perturbation data with AI models to predict genetic perturbation effects across cellular systems and disease contexts.

Identifiers

PMID41889931
PMCPMC13015719

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.