ArticleNPJ genomic medicine2026
GANomics: bridging legacy and modern transcriptomic platforms for clinical applications.
Article in NPJ genomic medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
The evolution of transcriptomic technologies requires effective translation between legacy and modern platforms to fully leverage historical data. We present GANomics, a generative adversarial network (GAN) framework that enables bidirectional translation between microarray and RNA-seq data using a small number of samples profiled by both technologies. By integrating paired and unpaired samples through a pair-aware feedback loss, GANomics enforces one-to-one transcript mappings while preserving global gene expression distributions. Applied to a neuroblastoma cohort (n = 498; 10,042 genes) and benchmarked against six alternative methods, GANomics achieved high per-sample correlations ( > 0.96) between real and synthetic data with as few as ten paired profiles. With fifty paired profiles, it accurately recapitulated differential expression, maintained pathway-level rankings, and enabled a cross-platform classifier to transfer comparable to real data. Consistent performance across five additional benchmark datasets confirmed its robustness. By bridging legacy and contemporary transcriptomic data while retaining biological consistency, GANomics facilitates scalable data integration for biomarker reuse and the expansion of transcriptomic resources in clinical applications.
Identifiers
What OpenQuestion 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 OpenQuestion graph.