Evidence map›Paper›PMID 42294313›Full record

ReviewFrontiers in oncology2026

Beyond counting: how single-cell long-read sequencing turns transcriptome complexity into precision targets.

Ashley Byrne, Colette Felton, William Stephenson

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Ashley Byrne *Department of Proteomic and Genomic Technologies, Genentech, South San Francisco, CA, United States.
Colette Felton *Department of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, CA, United States.
William StephensonDepartment of Proteomic and Genomic Technologies, Genentech, South San Francisco, CA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-seq) has emerged as a critical tool in oncology research, revealing key aspects of immune infiltration, tumor heterogeneity, and the tumor microenvironment. However, most scRNA-seq experiments capture only a portion of the 5'- or 3'-end of the gene due to limitations in sequencing read length. This limits short-read scRNA-seq to a method that quantifies gene expression but falls short of understanding the full complexity of the transcriptome. Since single nucleotide variants (SNVs), structural variants (SVs), and aberrant splicing are known drivers of tumor development, it is critical to be able to understand their heterogeneity at the single cell level. Long-read RNA-seq is capable of sequencing full-length molecules, simplifying the process of identifying these types of alterations. This review examines how single-cell long-read sequencing (scLRS) technologies are overcoming the limitations of short-read platforms to resolve the complexity of the cancer transcriptome. We highlight key applications that leverage full-length information, including the identification of novel tumor-specific neo-antigens and fusion genes. By linking genotype information with transcript expression, this technology holds the potential for developing highly specific, isoform-selective therapies that minimize off-target effects. We also describe the application of scLRS to sensitively trace tumor clone subtypes using isoform profiles and to identify clonal evolution through tracing SNV variation within single cells. Furthermore, we discuss the current state of the scLRS field and how it can be applied for multimodal analysis, which integrates full-length transcriptomics with genomic, spatial and proteomic data to create a more comprehensive profile of the tumor micro-environment. Finally, we outline the current technological and computational challenges of scLRS, including cost, throughput, and the need for standardized bioinformatic tools, providing a roadmap for future advancements. As these limitations are overcome, we foresee scLRS as an indispensable tool for uncovering the transcriptomic complexity within the tumor microenvironment, accelerating the development of precision oncology therapies.

Indexed as

alternative splicingdriver variantslong-read sequencingprecision oncologysingle cellspatial sequencingtranscriptomics

Identifiers

PMID42294313
PMCPMC13253305

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.