Evidence map›Paper›PMID 35459094›Full record

ArticleBMC bioinformatics2022

A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization.

Ying Ji, Rui Chen, Quan Wang, Qiang Wei, Ran Tao, Bingshan Li

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2022. 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
0.2field-weighted citation impact, top 52% of its field
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, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Ying JiDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37212, USA.
Rui ChenDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37212, USA.
Quan WangDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37212, USA.
Qiang WeiDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37212, USA.
Ran Tao *Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, TN, 37212, USA. r.tao@vumc.org.
Bingshan Li *Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37212, USA. bingshan.li@vanderbilt.edu.
Vanderbilt University · USVanderbilt University Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutism spectrum disorder (ASD) is a group of complex neurodevelopment disorders with a strong genetic basis. Large scale sequencing studies have identified over one hundred ASD risk genes. Nevertheless, the vast majority of ASD risk genes remain to be discovered, as it is estimated that more than 1000 genes are likely to be involved in ASD risk. Prioritization of risk genes is an effective strategy to increase the power of identifying novel risk genes in genetics studies of ASD. As ASD risk genes are likely to exhibit distinct properties from multiple angles, we reason that integrating multiple levels of genomic data is a powerful approach to pinpoint genuine ASD risk genes.

resultsWe present BNScore, a Bayesian model selection framework to probabilistically prioritize ASD risk genes through explicitly integrating evidence from sequencing-identified ASD genes, biological annotations, and gene functional network. We demonstrate the validity of our approach and its improved performance over existing methods by examining the resulting top candidate ASD risk genes against sets of high-confidence benchmark genes and large-scale ASD genome-wide association studies. We assess the tissue-, cell type- and development stage-specific expression properties of top prioritized genes, and find strong expression specificity in brain tissues, striatal medium spiny neurons, and fetal developmental stages.

conclusionsIn summary, we show that by integrating sequencing findings, functional annotation profiles, and gene-gene functional network, our proposed BNScore provides competitive performance compared to current state-of-the-art methods in prioritizing ASD genes. Our method offers a general and flexible strategy to risk gene prioritization that can potentially be applied to other complex traits as well.

Indexed as

Autism Spectrum DisorderAutistic DisorderBayes TheoremGene Regulatory NetworksGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansASD risk genesBayesian model selectionGene prioritization

Identifiers

PMID35459094
PMCPMC9034518
OpenAlexW4224210501

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.