Fusion gene discovery in single cells from high throughput long read single cell transcriptomes

High throughput long-read single cell RNA sequencing allows for fusion gene discovery in thousands of cells in parallel, which is however constrained by the lack of robust computational tools. Here, we develop LongFUSE that employs the XOR logic operation and stringent filtering criteria for the accurate detection of cell-specific fusion genes and their splicing isoforms. LongFUSE outperforms existing tools in both simulation and real data, demonstrating high accuracy and robustness.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-01-14
DOI
https://doi.org/10.64898/2026.01.13.699333
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
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article

Fusion gene discovery in single cells from high throughput long read single cell transcriptomes

bioRxiv (Cold Spring Harbor Laboratory)
Single-cell and spatial transcriptomics
article

Fusion gene discovery in single cells from high throughput long read single cell transcriptomes

article en

Abstract

High throughput long-read single cell RNA sequencing allows for fusion gene discovery in thousands of cells in parallel, which is however constrained by the lack of robust computational tools. Here, we develop LongFUSE that employs the XOR logic operation and stringent filtering criteria for the accurate detection of cell-specific fusion genes and their splicing isoforms. LongFUSE outperforms existing tools in both simulation and real data, demonstrating high accuracy and robustness.

bioRxiv (Cold Spring Harbor Laboratory)
Northwestern University (US), Emory University (US), Robert H. Lurie Comprehensive Cancer Center of Northwestern University
Openalex Percentile: Top 88%
Single-cell and spatial transcriptomics
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