SatuRn: Scalable analysis of differential transcript usage for bulk and single-cell RNA-sequencing applications

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

SatuRn : Scalable analysis of differential transcript usage for bulk and single-cell RNA-sequencing applications. / Gilis, Jeroen; Vitting-Seerup, Kristoffer; Van den Berge, Koen; Clement, Lieven.

In: F1000Research, Vol. 10, 374, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Gilis, J, Vitting-Seerup, K, Van den Berge, K & Clement, L 2022, 'SatuRn: Scalable analysis of differential transcript usage for bulk and single-cell RNA-sequencing applications', F1000Research, vol. 10, 374. https://doi.org/10.12688/f1000research.51749.2

APA

Gilis, J., Vitting-Seerup, K., Van den Berge, K., & Clement, L. (2022). SatuRn: Scalable analysis of differential transcript usage for bulk and single-cell RNA-sequencing applications. F1000Research, 10, [374]. https://doi.org/10.12688/f1000research.51749.2

Vancouver

Gilis J, Vitting-Seerup K, Van den Berge K, Clement L. SatuRn: Scalable analysis of differential transcript usage for bulk and single-cell RNA-sequencing applications. F1000Research. 2022;10. 374. https://doi.org/10.12688/f1000research.51749.2

Author

Gilis, Jeroen ; Vitting-Seerup, Kristoffer ; Van den Berge, Koen ; Clement, Lieven. / SatuRn : Scalable analysis of differential transcript usage for bulk and single-cell RNA-sequencing applications. In: F1000Research. 2022 ; Vol. 10.

Bibtex

@article{3111b453aa2d4f58af53feb93fa09303,
title = "SatuRn: Scalable analysis of differential transcript usage for bulk and single-cell RNA-sequencing applications",
abstract = "Alternative splicing produces multiple functional transcripts from a single gene. Dysregulation of splicing is known to be associated with disease and as a hallmark of cancer. Existing tools for differential transcript usage (DTU) analysis either lack in performance, cannot account for complex experimental designs or do not scale to massive single-cell transcriptome sequencing (scRNA-seq) datasets. We introduce satuRn, a fast and flexible quasi-binomial generalized linear modelling framework that is on par with the best performing DTU methods from the bulk RNA-seq realm, while providing good false discovery rate control, addressing complex experimental designs, and scaling to scRNA-seq applications.",
keywords = "Differential transcript usage, RNA-seq, SatuRn, Single-cell transcriptomics, Splicing, Statistical framework",
author = "Jeroen Gilis and Kristoffer Vitting-Seerup and {Van den Berge}, Koen and Lieven Clement",
note = "Publisher Copyright: {\textcopyright} 2022 Gilis J et al.",
year = "2022",
doi = "10.12688/f1000research.51749.2",
language = "English",
volume = "10",
journal = "F1000Research",
issn = "2046-1402",
publisher = "F1000Research",

}

RIS

TY - JOUR

T1 - SatuRn

T2 - Scalable analysis of differential transcript usage for bulk and single-cell RNA-sequencing applications

AU - Gilis, Jeroen

AU - Vitting-Seerup, Kristoffer

AU - Van den Berge, Koen

AU - Clement, Lieven

N1 - Publisher Copyright: © 2022 Gilis J et al.

PY - 2022

Y1 - 2022

N2 - Alternative splicing produces multiple functional transcripts from a single gene. Dysregulation of splicing is known to be associated with disease and as a hallmark of cancer. Existing tools for differential transcript usage (DTU) analysis either lack in performance, cannot account for complex experimental designs or do not scale to massive single-cell transcriptome sequencing (scRNA-seq) datasets. We introduce satuRn, a fast and flexible quasi-binomial generalized linear modelling framework that is on par with the best performing DTU methods from the bulk RNA-seq realm, while providing good false discovery rate control, addressing complex experimental designs, and scaling to scRNA-seq applications.

AB - Alternative splicing produces multiple functional transcripts from a single gene. Dysregulation of splicing is known to be associated with disease and as a hallmark of cancer. Existing tools for differential transcript usage (DTU) analysis either lack in performance, cannot account for complex experimental designs or do not scale to massive single-cell transcriptome sequencing (scRNA-seq) datasets. We introduce satuRn, a fast and flexible quasi-binomial generalized linear modelling framework that is on par with the best performing DTU methods from the bulk RNA-seq realm, while providing good false discovery rate control, addressing complex experimental designs, and scaling to scRNA-seq applications.

KW - Differential transcript usage

KW - RNA-seq

KW - SatuRn

KW - Single-cell transcriptomics

KW - Splicing

KW - Statistical framework

U2 - 10.12688/f1000research.51749.2

DO - 10.12688/f1000research.51749.2

M3 - Journal article

C2 - 36762203

AN - SCOPUS:85147555385

VL - 10

JO - F1000Research

JF - F1000Research

SN - 2046-1402

M1 - 374

ER -

ID: 343299032