Evidence map›Paper›PMID 39613793›Full record

ArticleNature communications2024

Multimodal analysis of RNA sequencing data powers discovery of complex trait genetics.

Daniel Munro, Nava Ehsan, Seyed Mehdi Esmaeili-Fard, Alexander Gusev, Abraham A Palmer, Pejman Mohammadi

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Daniel MunroDepartment of Psychiatry, UC San Diego, La Jolla, CA, USA.ORCID 0000-0002-0724-218X
Nava EhsanDepartment of Integrative Structural and Computational Biology, Scripps Research, La Jolla, CA, USA.ORCID 0000-0001-7453-2518
Seyed Mehdi Esmaeili-FardCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA, USA.ORCID 0000-0001-7509-5030
Alexander GusevDivision of Population Sciences, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA. alexander_gusev@dfci.harvard.edu.ORCID 0000-0002-7980-4620
Abraham A PalmerDepartment of Psychiatry, UC San Diego, La Jolla, CA, USA. aap@ucsd.edu.ORCID 0000-0003-3634-0747
Pejman MohammadiCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA, USA. pejmanm@uw.edu.ORCID 0000-0003-4457-8552

Funding

Sequencing CoreP50DA037844 · NIDA · UNIVERSITY OF CHICAGO · PI PALMER, ABRAHAM A · 2014 to 2023
$27.4M
SINGLE-CELL MULTI-OMIC APPROACHES TO MECHANISTICALLY CHARACTERIZE PSYCHIATRIC DISORDER RISK LOCI IN THE HUMAN BRAINR01MH125252 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUO, CHONGYUAN · 2021 to 2025
$3.7M
Haplotype-aware models of gene and isoform expression with application to genetic studies of disease in diverse populationsR01GM140287 · NIGMS · SEATTLE CHILDREN'S HOSPITAL · PI GAMAZON, ERIC R, MOHAMMADI, PEJMAN · 2021 to 2024
$2.8M
NIDA NIH HHS P50 DA037844NIGMS NIH HHS R01 GM140287NIMH NIH HHS R01 MH125252U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM140287U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R01MH125252U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) P50DA037844
6 · The paper itself

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.

Indexed as

PhenotypeQuantitative Trait LociSequence Analysis, RNAGene Expression RegulationGenome-Wide Association StudyHumansMultifactorial Inheritance

Identifiers

PMID39613793
PMCPMC11607376

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.