Evidence map›Paper›PMID 34669946›Full record

ArticleNucleic acids research2022

webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study.

Chen Cao, Jianhua Wang, Devin Kwok, Feifei Cui, Zilong Zhang, Da Zhao, Mulin Jun Li, Quan Zou

Abstract read
In one paragraph

Article in Nucleic acids research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 113 papers.

0numbers the graph read from it
0cells of the map it votes in
113citing 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

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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

113 citing papers in PubMed.

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  17. lncRNA localization and feature interpretability analysis.Molecular therapy. Nucleic acids · 2025
    Article
  18. Cancer Drug Sensitivity Prediction Based on Deep Transfer Learning.International journal of molecular sciences · 2025
    Article
  19. Review
  20. Article

53 more citing papers are in PubMed but not listed here.

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

8 authors.

Chen CaoYangtze Delta Region Institute (Quzhou), University of Electronic Science and Technology of China, Quzhou, China.ORCID 0000-0001-5343-808X
Jianhua WangDepartment of Pharmacology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Devin KwokSchool of Computer Science, McGill University, Montreal, Canada.
Feifei CuiYangtze Delta Region Institute (Quzhou), University of Electronic Science and Technology of China, Quzhou, China.
Zilong ZhangYangtze Delta Region Institute (Quzhou), University of Electronic Science and Technology of China, Quzhou, China.ORCID 0000-0002-4934-1258
Da ZhaoYangtze Delta Region Institute (Quzhou), University of Electronic Science and Technology of China, Quzhou, China.
Mulin Jun LiDepartment of Pharmacology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Quan ZouYangtze Delta Region Institute (Quzhou), University of Electronic Science and Technology of China, Quzhou, China.ORCID 0000-0001-6406-1142

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of transcriptome-wide association studies (TWAS) has enabled researchers to better identify and interpret causal genes in many diseases. However, there are currently no resources providing a comprehensive listing of gene-disease associations discovered by TWAS from published GWAS summary statistics. TWAS analyses are also difficult to conduct due to the complexity of TWAS software pipelines. To address these issues, we introduce a new resource called webTWAS, which integrates a database of the most comprehensive disease GWAS datasets currently available with credible sets of potential causal genes identified by multiple TWAS software packages. Specifically, a total of 235 064 gene-diseases associations for a wide range of human diseases are prioritized from 1298 high-quality downloadable European GWAS summary statistics. Associations are calculated with seven different statistical models based on three popular and representative TWAS software packages. Users can explore associations at the gene or disease level, and easily search for related studies or diseases using the MeSH disease tree. Since the effects of diseases are highly tissue-specific, webTWAS applies tissue-specific enrichment analysis to identify significant tissues. A user-friendly web server is also available to run custom TWAS analyses on user-provided GWAS summary statistics data. webTWAS is freely available at http://www.webtwas.net.

Indexed as

Databases, GeneticGenetic Predisposition to DiseaseGene Expression ProfilingGenetic Association StudiesGenetic Diseases, InbornGenome-Wide Association StudyHumansPolymorphism, Single NucleotideQuantitative Trait LociSoftwareTranscriptome

Identifiers

PMID34669946
PMCPMC8728162

What Socratic holds

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LicenceCC BY
Read underepoch 390

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 Socratic graph.