Back to search

Article

A comprehensive benchmark of transcriptome-wide fusion detection using long-read RNA sequencing

2026-08-12

Abstract excerpt

Fusion transcripts contribute to cancer, inherited diseases, developmental disorders, and evolution. Long-read RNA sequencing enables direct sequencing of full-length transcripts, creating new opportunities to detect complex fusion architectures, including previously inaccessible multi-segmented fusion transcripts. However, accurate transcriptome-wide fusion detection remains challenging because existing methods s...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
8279ab2a-2ac3-586b-b1b5-a2065a8d5c12
DOI
10.64898/2026.08.07.743439
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
A comprehensive benchmark of transcriptome-wide fusion detection using long-read RNA sequencingDOI 10.64898/2026.08.07.743439
Select a neighboring publication to make it the new centre.