NGS-based approaches for detecting fusion transcripts have greatly improved our understanding of the molecular basis of cancer.

Single-cell technologies, particularly single-cell RNA sequencing (scRNA-seq) methods, have revolutionized drug discovery and development by providing unprecedented insights into cellular heterogeneity and gene expression at the single-cell level.

The workflow of viral metagenomics includes sample collection, virus‐like particle purification, nucleic acid extraction, library preparation, and metagenomics sequencing.

The emergence of virome sequencing has opened up a world of possibilities, allowing researchers to delve into the hidden dimensions of viral diversity and its profound implications.