Authors
Jian Zou, Yannick Düren, Xinyi Wang, Ying Xiang, Yunhui Qi, Miao Wang, Yilin Wu, Samuel Singer, Li-Xuan Qin
Published in
bioRxiv : the preprint server for biology. Aug 14, 2026. Epub Aug 14, 2026.
Abstract
Reliable translation of microRNA sequencing data depends on effective harmonization to mitigate artifacts from variable experimental handling. Although many harmonization methods exist, prior evaluations have focused mainly on differential expression analysis, leaving the impact on subgroup discovery understudied. We present a framework for evaluating harmonization in the context of sample clustering, which integrates AI-augmented datasets, statistical evaluation pipelines, and accessible software tools, enabling systematic comparisons across diverse signal-to-artifact ratios and cluster composition settings. Using this framework, we show that harmonization can, often partially, restore clustering accuracy lost to artifacts, especially at moderate signal-to-artifact ratios, with the level of gains depending on the specific harmonization method, the paired clustering technique, and the cluster composition setting. We further confirm these findings by analyzing reconstructed cohorts from The Cancer Genome Atlas breast cancer microRNA sequencing data. Collectively, the results underscore the need for tailored harmonization to support reliable subgroup discovery and highlight the broader importance of context-specific workflows in translational genomics.
PMID:
42845360
Bibliographic data and abstract were imported from PubMed on 08 Oct 2026.
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