Singletrome enhances detection of long noncoding RNAs in single cell transcriptomes

Single cell RNA sequencing (scRNA-seq) has revolutionized the study of gene expression in individual cell types, but scRNA-seq studies have focused primarily on expression of protein-coding genes. Long noncoding RNAs (lncRNAs) are more diverse than protein-coding genes, yet remain underexplored in part because they are underrepresented in reference annotations applied to scRNA-seq. Merging annotations containing protein-coding and lncRNA genes is not sufficient, because the addition of lncRNA genes that overlap in sense and antisense with protein-coding genes will affect how reads are counted for both protein-coding and lncRNA genes. Here, we introduce Singletrome, a Singularity image that integrates protein-coding and lncRNA gene transfer format (GTF) annotations to generate enhanced annotations that take into account the sense and antisense overlap of annotated genes, maps scRNA-seq data, and produces files for downstream analysis and visualization. With Singletrome, we detected thousands of lncRNAs not included in GENCODE, clustered cell types based solely on lncRNA expression, and demonstrated that machine learning can predict cell type and disease through lncRNAs alone. This comprehensive annotation will allow mapping of lncRNA expression across cell types of the human body, facilitating the development of an atlas of human lncRNAs in health and disease with the ability to integrate new lncRNA annotations as they become available.

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Publication Details

Journal
Scientific Reports
Published
2025-08-12
DOI
https://doi.org/10.1038/s41598-025-13528-9
Citations
4
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
3.75

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article

Singletrome enhances detection of long noncoding RNAs in single cell transcriptomes

Robert P. Sparks, Alan C. Mullen, Raza‐Ur Rahman, Iftikhar Ahmad et al.
4 citations
Scientific Reports
Cancer-related molecular mechanisms research
3.75
article

Singletrome enhances detection of long noncoding RNAs in single cell transcriptomes

Robert P. Sparks, Alan C. Mullen, Raza‐Ur Rahman, Iftikhar Ahmad, Amel Ben Saad, Zixiu Li
article en
4 citations

Abstract

Single cell RNA sequencing (scRNA-seq) has revolutionized the study of gene expression in individual cell types, but scRNA-seq studies have focused primarily on expression of protein-coding genes. Long noncoding RNAs (lncRNAs) are more diverse than protein-coding genes, yet remain underexplored in part because they are underrepresented in reference annotations applied to scRNA-seq. Merging annotations containing protein-coding and lncRNA genes is not sufficient, because the addition of lncRNA genes that overlap in sense and antisense with protein-coding genes will affect how reads are counted for both protein-coding and lncRNA genes. Here, we introduce Singletrome, a Singularity image that integrates protein-coding and lncRNA gene transfer format (GTF) annotations to generate enhanced annotations that take into account the sense and antisense overlap of annotated genes, maps scRNA-seq data, and produces files for downstream analysis and visualization. With Singletrome, we detected thousands of lncRNAs not included in GENCODE, clustered cell types based solely on lncRNA expression, and demonstrated that machine learning can predict cell type and disease through lncRNAs alone. This comprehensive annotation will allow mapping of lncRNA expression across cell types of the human body, facilitating the development of an atlas of human lncRNAs in health and disease with the ability to integrate new lncRNA annotations as they become available.

Scientific ReportsVol. 15(1)
Broad Institute (US), University of Massachusetts Chan Medical School (US), University of Applied Sciences Potsdam (DE), Software (Germany) (DE), Massachusetts Institute of Technology (US)
National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases
Openalex Percentile: Top 6%
Cancer-related molecular mechanisms research
3.75
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