ASET: an end-to-end pipeline for quantification and visualization of allele specific expression

Allele-specific expression (ASE) analyses from RNA-Seq data provide quantitative insights into genomic imprinting and the genetic variants that affect transcription. Robust ASE analysis requires the integration of multiple computational steps, including read alignment, read counting, data visualization, and statistical testing-this complexity creates challenges for reproducibility, scalability, and ease of use. Here, we present ASE Toolkit (ASET), an end-to-end pipeline that streamlines SNP-level ASE data generation, visualization, and testing for parent-of-origin (PofO) effect. ASET includes a modular pipeline built with Nextflow for ASE quantification from short-read transcriptome sequencing reads, an R library for data visualization, and a Julia script for PofO testing. ASET performs comprehensive read quality control, SNP-tolerant alignment to reference genomes, read counting with allele and strand resolution, annotation with genes and exons, and estimation of contamination. In sum, ASET provides a complete and easy-to-use solution for molecular and biomedical scientists to identify and interpret patterns of ASE from RNA-Seq data.

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Publication Details

Journal
BMC Bioinformatics
Published
2025-10-21
DOI
https://doi.org/10.1186/s12859-025-06282-2
Primary Topic
Genetic Syndromes and Imprinting
Type
article
Field-Weighted Citation Impact
0.00

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article

ASET: an end-to-end pipeline for quantification and visualization of allele specific expression

Kerby Shedden, Beverly I. Strassmann, Claudius Vincenz, Chris Gates et al.
BMC Bioinformatics
Genetic Syndromes and Imprinting
article

ASET: an end-to-end pipeline for quantification and visualization of allele specific expression

Kerby Shedden, Beverly I. Strassmann, Claudius Vincenz, Chris Gates, Wei-Sheng Wu
article en

Abstract

Allele-specific expression (ASE) analyses from RNA-Seq data provide quantitative insights into genomic imprinting and the genetic variants that affect transcription. Robust ASE analysis requires the integration of multiple computational steps, including read alignment, read counting, data visualization, and statistical testing-this complexity creates challenges for reproducibility, scalability, and ease of use. Here, we present ASE Toolkit (ASET), an end-to-end pipeline that streamlines SNP-level ASE data generation, visualization, and testing for parent-of-origin (PofO) effect. ASET includes a modular pipeline built with Nextflow for ASE quantification from short-read transcriptome sequencing reads, an R library for data visualization, and a Julia script for PofO testing. ASET performs comprehensive read quality control, SNP-tolerant alignment to reference genomes, read counting with allele and strand resolution, annotation with genes and exons, and estimation of contamination. In sum, ASET provides a complete and easy-to-use solution for molecular and biomedical scientists to identify and interpret patterns of ASE from RNA-Seq data.

BMC BioinformaticsVol. 26(1)
University of Michigan (US), Institute for Social Research (NO)
John Templeton Foundation, University of Michigan, National Institutes of Health
Openalex Percentile: Top 68%
Genetic Syndromes and Imprinting
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