PETScan: score-based genome-wide association analysis of RNA-Seq and ATAC-Seq data.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41719189.
- Also identified by DOI 10.1093/bioinformatics/btaf672 and PMC identifier 12930850.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
High-dimensional sequencing data, such as RNA-Seq for gene expression and ATAC-Seq for chromatin accessibility, are widely used in studying systems biology. Accessible chromatin allows transcription factors and regulatory elements to bind to DNA, thereby regulating transcription through the activation or repression of target genes. The association analysis of RNA-Seq and ATAC-Seq data provides insights into gene regulatory mechanisms. Most existing analytic tools exclusively focus on cis-associations, despite regulatory elements being able to physically interact with distant target genes. Furthermore, conventional approaches often utilize Pearson or Spearman correlations, which ignore the count-based nature of RNA-Seq data. To address these limitations, we introduce PETScan, a computationally efficient genome-wide PEak-Transcript Score-based association analysis, utilizing negative binomial models to better accommodate RNA-Seq data. We leverage score tests and matrix calculations for improved computational efficiency, and combine an empirical permutation method with genomic control to ensure valid p-value calculations in studies with limited sample sizes. In real-world datasets, PETScan achieved three orders of magnitude faster than Wald tests, while identifying similar significant gene-peak pairs. The PETScan R package is available on GitHub at https://github.com/yajing-hao/PETScan.
Medical subject headings
- Software
- Genome-Wide Association Study
- RNA-Seq
- Chromatin Immunoprecipitation Sequencing
- Sequence Analysis, RNA