ReviewJournal of advanced research2026
Advances in high-throughput drug screening based on pharmacotranscriptomics.
Review in Journal of advanced research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Applying biotechnology to overcome cancer drug resistance and improve public health outcomes.Osong public health and research perspectives · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundDrug screening constitutes the predominant paradigm for novel drug discovery. With the development of omics, drug screening has gradually developed into pharmacotranscriptomics-based drug screening (PTDS), which is different from target-based and phenotype-based drug screening. PTDS is a rapidly evolving interdisciplinary field that concurrently demands overcoming large-scale pharmacotranscriptomics profiling and computational challenges inherent to high-dimensional feature data. AIM OF REVIEW: This review aims to summarize the developmental trajectory and research advancements in PTDS, with a focus on large-scale pharmacotranscriptomics profiling and artificial intelligence-driven data mining. It elucidates the appropriate application fields of PTDS in comparison to traditional drug screening paradigms, thereby providing novel perspectives for the technological evolution and implementation of PTDS. Key scientific concepts of review: PTDS can detect gene expression changes following drug perturbation in cells on a large scale and analyze the efficacy of drug-regulated gene sets, signaling pathways, and even complex diseases by combining artificial intelligence. The technical evolution of PTDS is systematically summarized, encompassing advancements in high-throughput PTDS detection technologies and data analysis methods. PTDS is categorized into microarray, targeted transcriptomics, and RNA-seq. Data analysis of PTDS involves ranking, unsupervised learning, and supervised learning algorithms. All these methods remain active in research and industry, coexisting to address evolving drug screening needs. On this basis, the roles of PTDS in promoting pathway-based drug screening strategies are deeply explored for drug discovery and drug combination design. Meanwhile, we also focus on the application of PTDS in screening and mechanism analysis of traditional Chinese medicine (TCM), which reflects that PTDS is suitable for detecting the complex efficacy of drugs, especially TCM. PTDS is an important development direction for high-throughput screening. By combining with artificial intelligence, PTDS will greatly revolutionize our understanding of drug screening and promote new drug research and development.
Indexed as
Identifiers
What Socratic holds
Registered trials
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.