Evidence map›Paper›PMID 39282456›Full record

ArticlebioRxiv : the preprint server for biology2024

A Deep Dive into Statistical Modeling of RNA Splicing QTLs Reveals New Variants that Explain Neurodegenerative Disease.

David Wang, Matthew R Gazzara, San Jewell, Benjamin Wales-McGrath, Christopher D Brown, Peter S Choi, Yoseph Barash

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

David WangDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania.ORCID 0000-0002-1566-5123
Matthew R GazzaraDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania.ORCID 0000-0001-7710-4551
San JewellDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania.ORCID 0000-0002-6494-8015
Benjamin Wales-McGrathDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania.ORCID 0009-0006-4184-7875
Christopher D BrownDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania.
Peter S ChoiDepartment of Pathology & Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania.ORCID 0000-0002-2820-3032
Yoseph BarashDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania.ORCID 0000-0003-3005-5048

Funding

Methods for RNA splicing variations detection, quantification, visualization, and association from large heterogeneous datasetsR01GM128096 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI BARASH, YOSEPH · 2018 to 2021
$1.8M
Methods for improving clinical diagnostic by detection, prediction, interpretation and prioritization of aberrant transcriptome variationsR01LM013437 · NLM · UNIVERSITY OF PENNSYLVANIA · PI BARASH, YOSEPH · 2020 to 2023
$1.4M
Mechanisms and consequences of 3'UTR isoform diversity in erythropoiesisF31HL162546 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI GAZZARA, MATTHEW ROBERT · 2022 to 2024
$136k
Developing Machine Learning Models for the Analysis of Splicing Data in Large Heterogeneous CohortsF31CA265218 · NCI · UNIVERSITY OF PENNSYLVANIA · PI WANG, DAVID · 2021 to 2023
$121k
NCI NIH HHS F31 CA265218NHLBI NIH HHS F31 HL162546NIGMS NIH HHS R01 GM128096NLM NIH HHS R01 LM013437
6 · The paper itself

Abstract

Genome-wide association studies (GWAS) have identified thousands of putative disease causing variants with unknown regulatory effects. Efforts to connect these variants with splicing quantitative trait loci (sQTLs) have provided functional insights, yet sQTLs reported by existing methods cannot explain many GWAS signals. We show current sQTL modeling approaches can be improved by considering alternative splicing representation, model calibration, and covariate integration. We then introduce MAJIQTL, a new pipeline for sQTL discovery. MAJIQTL includes two new statistical methods: a weighted multiple testing approach for sGene discovery and a model for sQTL effect size inference to improve variant prioritization. By applying MAJIQTL to GTEx, we find significantly more sGenes harboring sQTLs with functional significance. Notably, our analysis implicates the novel variant rs582283 in Alzheimer's disease. Using antisense oligonucleotides, we validate this variant's effect by blocking the implicated YBX3 binding site, leading to exon skipping in the gene MS4A3.

Identifiers

PMID39282456
PMCPMC11398334

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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.