Demo Data from VLDB 2026 / reviewers in the wild / expert
Jonathan Bradley
dblp:424/4016
· DBLP profile ↗
1ranked-venue papers
0as first author
1since 2021 · last 2021
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 93% Medical and health informatics · 7% |
Topics — the 5 heaviest of 5, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › epigenomics
DNA methylation |
0.5 | 1 | 2021 | A gene-level methylome-wide association analysis identifies novel Alzheimer's disease genes · Bioinform. 2021 |
Bioinformatics and computational biology
epigenomics |
0.5 | 1 | 2021 | A gene-level methylome-wide association analysis identifies novel Alzheimer's disease genes · Bioinform. 2021 |
Bioinformatics and computational biology › genomics
genome-wide association study |
0.5 | 1 | 2021 | A gene-level methylome-wide association analysis identifies novel Alzheimer's disease genes · Bioinform. 2021 |
Bioinformatics and computational biology › statistical genetics › post-GWAS analysis
transcriptome-wide association study |
0.5 | 1 | 2021 | A gene-level methylome-wide association analysis identifies novel Alzheimer's disease genes · Bioinform. 2021 |
Medical and health informatics
alzheimer's disease genetics |
0.1 | 1 | 2021 | A gene-level methylome-wide association analysis identifies novel Alzheimer's disease genes · Bioinform. 2021 |
Methods — techniques the papers use, named apart from their topics
summary statistics integration · 0.5omnibus test · 0.5
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2021 | A gene-level methylome-wide association analysis identifies novel Alzheimer's disease genesabstractAbstract Motivation Transcriptome-wide association studies (TWAS) have successfully facilitated the discovery of novel genetic risk loci for many complex traits, including late-onset Alzheimer’s disease (AD). However, most existing TWAS methods rely only on gene expression and ignore epigenetic modification (i.e. DNA methylation) and functional regulatory information (i.e. enhancer-promoter interactions), both of which contribute significantly to the genetic basis of AD. Results We develop a novel gene-level association testing method that integrates genetically regulated DNA methylation and enhancer–target gene pairs with genome-wide association study (GWAS) summary results. Through simulations, we show that our approach, referred to as the CMO (cross methylome omnibus) test, yielded well controlled type I error rates and achieved much higher statistical power than competing methods under a wide range of scenarios. Furthermore, compared with TWAS, CMO identified an average of 124% more associations when analyzing several brain imaging-related GWAS results. By analyzing to date the largest AD GWAS of 71 880 cases and 383 378 controls, CMO identified six novel loci for AD, which have been ignored by competing methods. Availabilityand implementation The data used in this work were obtained from the following publicly available datasets: IGAP1, GWAX, UK Biobank, a 2019 meta-analyzed AD GWAS results and a imaging-derived phenotype GWAS results. The data resources are summarized in Supplementary Table S7. We used the publicly available software and tools for competing methods. All codes used to generate results that are reported in this manuscript and software for our newly proposed method CMO are available at https://github.com/ChongWuLab/CMO. Supplementary information Supplementary data are available at Bioinformatics online. Jonathan Bradley, Hong-Wen Deng |
Bioinform. | 2 |