Evidence map›Paper›PMID 40861396›Full record

ArticleBioinformatics advances2025

smartSim: simulation of splice aware single cell smart-seq3 data.

Marie Van Hecke, Kathleen Marchal

Abstract read
In one paragraph

Article in Bioinformatics advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Marie Van HeckeIDLab, Department of Information Technology, Ghent University-imec, 9052 Ghent, Belgium.ORCID https://orcid.org/0000-0002-2397-8269
Kathleen MarchalIDLab, Department of Information Technology, Ghent University-imec, 9052 Ghent, Belgium.ORCID https://orcid.org/0000-0002-2169-4588

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Smart-seq3 is a powerful full-length single-cell RNA sequencing protocol that enables transcript-level quantification and splicing analysis by preserving unique molecular identifier (UMI) information. However, benchmarking computational tools for isoform reconstruction and splicing quantification remains challenging due to the lack of ground truth datasets. Herein, we present smartSim, a Smart-seq3 read simulator designed to generate realistic sequencing data that accurately reflects the complexities of single-cell transcriptomics. Results: smartSim simulates known and novel splicing events, generates both UMI-containing and internal reads, and mimics protocol-specific biases by leveraging empirical data distributions. Our results show that smartSim-generated data closely resembles real Smart-seq3 datasets in terms of fragment length distributions, internal read counts, and read quality scores. It generates raw sequencing reads in FASTQ format, making it compatible with both genome- and transcriptome-based alignment tools. By extending simulation beyond gene-level quantification, smartSim provides a crucial resource for evaluating and improving computational methods for alternative splicing detection and isoform reconstruction in single-cell RNA sequencing. Availability and implementation: smartSim is available at https://github.com/MarchalLab/smartSim.

Identifiers

PMID40861396
PMCPMC12373632

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LicenceCC BY
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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.