Evidence mapPaperPMID 41968138Full record

ArticleScientific reports2026

Advancing target discovery through disease-specific integration of multi-modal target identification models and comprehensive benchmarking system.

Howell Leung, Chengchen Duan, Wenhao Gou, Jianjiu Chen, Ying Xin, Zetian Zheng, Vladimir Naumov, David Gennert, Man Zhang, Alex Aliper and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 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

14 authors.

Howell Leung *Insilico Medicine Hong Kong Ltd, Hong Kong Science and Technology Park, Unit 310, 3/F, Building 8W, Hong Kong SAR, China.
Chengchen Duan *Insilico Medicine Hong Kong Ltd, Hong Kong Science and Technology Park, Unit 310, 3/F, Building 8W, Hong Kong SAR, China.
Wenhao Gou *Insilico Medicine Hong Kong Ltd, Hong Kong Science and Technology Park, Unit 310, 3/F, Building 8W, Hong Kong SAR, China.
Jianjiu ChenInsilico Medicine Hong Kong Ltd, Hong Kong Science and Technology Park, Unit 310, 3/F, Building 8W, Hong Kong SAR, China.
Ying XinInsilico Medicine Hong Kong Ltd, Hong Kong Science and Technology Park, Unit 310, 3/F, Building 8W, Hong Kong SAR, China.
Zetian ZhengInsilico Medicine Hong Kong Ltd, Hong Kong Science and Technology Park, Unit 310, 3/F, Building 8W, Hong Kong SAR, China.
Vladimir NaumovInsilico Medicine AI Ltd, Level 6, Unit 08, Block A, IRENA HQ Building, Masdar City, Abu Dhabi, United Arab Emirates.
David GennertInsilico Medicine US Inc, 1000 Massachusetts Avenue, Suite 126, Cambridge, MA, 02138, USA.
Man ZhangInsilico Medicine Shanghai Ltd, 9 F, Chamtime Plaza Block C, Lane 2889, Jinke Road, Pudong New Area, China.
Alex AliperInsilico Medicine AI Ltd, Level 6, Unit 08, Block A, IRENA HQ Building, Masdar City, Abu Dhabi, United Arab Emirates.
Feng RenInsilico Medicine Hong Kong Ltd, Hong Kong Science and Technology Park, Unit 310, 3/F, Building 8W, Hong Kong SAR, China.
Evgeny IzumchenkoDepartment of Medicine, Section of Hematology and Oncology, University of Chicago, Chicago, IL, USA.
Frank W PunInsilico Medicine Hong Kong Ltd, Hong Kong Science and Technology Park, Unit 310, 3/F, Building 8W, Hong Kong SAR, China. frank.pun@insilico.com.
Alex ZhavoronkovInsilico Medicine Hong Kong Ltd, Hong Kong Science and Technology Park, Unit 310, 3/F, Building 8W, Hong Kong SAR, China. alex@insilico.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Target identification is crucial for drug development. AI-driven approaches leveraging multi-omics and computational modeling can accelerate this process. However, integrating multi-modal data for disease-specific target identification and predicting translational potential remains challenging. Moreover, the absence of a systematic evaluation framework for model performance limits confidence in target reliability. This study presents a unified framework combining machine learning-based target identification with comprehensive benchmarking. We first developed Target Identification Pro (TargetPro), a disease-specific model spanning 38 diseases across oncology, metabolic, immune, fibrotic, and neurological categories. TargetPro shows strong predictive performance for clinical-stage targets and reveals disease-specific patterns, underscoring the need for tailored target detection models. We next created Target Identification Benchmark (TargetBench 1.0) to assess target identification systems, including large language models, based on their ability to recover established targets and find high-quality novel candidates. This integrated approach offers a streamlined strategy to evaluate target discovery models, ultimately improving drug development efficiency.

Indexed as

BenchmarkingDrug DevelopmentDrug DiscoveryHumansLarge Language ModelsMachine Learning

Identifiers

PMID41968138
PMCPMC13230693

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.