Transcriptomic Harmonization as the Way for Suppressing Cross-Platform Bias and Batch Effect

(1) Background: Emergence of methods interrogating gene expression at high throughput gave birth to quantitative transcriptomics, but also posed a question of inter-comparison of expression profiles obtained using different equipment and protocols and/or in different series of experiments. Addressing this issue is challenging, because all of the above variables can dramatically influence gene expression signals and, therefore, cause a plethora of peculiar features in the transcriptomic profiles. Millions of transcriptomic profiles were obtained and deposited in public databases of which the usefulness is however strongly limited due to the inter-comparison issues; (2) Methods: Dozens of methods and software packages that can be generally classified as either flexible or predefined format harmonizers have been proposed, but none has become to the date the gold standard for unification of this type of Big Data; (3) Results: However, recent developments evidence that platform/protocol/batch bias can be efficiently reduced not only for the comparisons of limited transcriptomic datasets. Instead, instruments were proposed for transforming gene expression profiles into the universal, uniformly shaped format that can support multiple inter-comparisons for reasonable calculation costs. This forms a basement for universal indexing of all or most of all types of RNA sequencing and microarray hybridization profiles; (4) Conclusions: In this paper, we attempted to overview the landscape of modern approaches and methods in transcriptomic harmonization and focused on the practical aspects of their application.

Automated summary

The emergence of high throughput gene expression methods has led to the development of quantitative transcriptomics, but also raised the question of comparing expression profiles obtained from different equipment, protocols, and/or experiments. Various methods have been proposed to address this issue, but there is no gold standard for unifying this type of Big Data. Recent developments have shown that platform/protocol/batch bias can be efficiently reduced, allowing for the transformation of gene expression profiles into a universal format that supports multiple inter-comparisons at a reasonable cost. This paves the way for the universal indexing of RNA sequencing and microarray hybridization profiles.