Multimodal Analysis of RNA Sequencing Data Powers Discovery of Complex Trait Genetics
NATURE COMMUNICATIONS(2024)
Univ Calif San Diego | Scripps Res | Seattle Childrens Res Inst | Dana Farber Canc Inst
Abstract
RNA sequencing has the potential to reveal many modalities of transcriptional regulation, such as various splicing phenotypes, but studies on gene regulation are often limited to gene expression due to the complexity of extracting and analyzing multiple RNA phenotypes. Here, we present Pantry, a framework to efficiently generate diverse RNA phenotypes from RNA sequencing data and perform downstream integrative analyses with genetic data. Pantry generates phenotypes from six modalities of transcriptional regulation (gene expression, isoform ratios, splice junction usage, alternative TSS/polyA usage, and RNA stability) and integrates them with genetic data via QTL mapping, TWAS, and colocalization testing. We apply Pantry to Geuvadis and GTEx data, finding that 4768 of the genes with no identified eQTL in Geuvadis have QTL in at least one other transcriptional modality, resulting in a 66% increase in genes over eQTL mapping. We further found that the QTL exhibit modality-specific functional properties that are further reinforced by joint analysis of different RNA modalities. We also show that generalizing TWAS to multiple RNA modalities approximately doubles the discovery of unique gene-trait associations, and enhances identification of regulatory mechanisms underlying GWAS signal in 42% of previously associated gene-trait pairs. Here, the authors present the Pantry framework, which extracts features from RNA sequencing data and performs multimodal genetic analyses. This type of analysis can increase gene-trait associations identified compared to using only expression levels.
MoreTranslated text
PDF
View via Publisher
AI Read Science
Must-Reading Tree
Example

Generate MRT to find the research sequence of this paper
Related Papers
Featurecounts: an Efficient General Purpose Program for Assigning Sequence Reads to Genomic Features
2013
被引用22993 | 浏览
2009
被引用220 | 浏览
2014
被引用2072 | 浏览
2014
被引用2223 | 浏览
2019
被引用304 | 浏览
2018
被引用331 | 浏览
2019
被引用405 | 浏览
2019
被引用394 | 浏览
2019
被引用91 | 浏览
2023
被引用47 | 浏览
2024
被引用1 | 浏览
2024
被引用8 | 浏览
2023
被引用7 | 浏览
Data Disclaimer
The page data are from open Internet sources, cooperative publishers and automatic analysis results through AI technology. We do not make any commitments and guarantees for the validity, accuracy, correctness, reliability, completeness and timeliness of the page data. If you have any questions, please contact us by email: report@aminer.cn
Chat Paper
去 AI 文献库 对话