Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Jialin Qu

dblp:316/4322 · DBLP profile ↗
← Back
1ranked-venue papers
1as first author
1since 2021 · last 2022
—ORCID · unresolved

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 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 · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › functional genomics › functional enrichment analysis
gene set enrichment analysis
0.612022
Gene set analysis with graph-embedded kernel association test · Bioinform. 2022
Bioinformatics and computational biology › statistical genetics › association testing
kernel association test
0.612022
Gene set analysis with graph-embedded kernel association test · Bioinform. 2022
Bioinformatics and computational biology › genomics › genome-wide association study
pathway-based association analysis
0.612022
Gene set analysis with graph-embedded kernel association test · Bioinform. 2022

Methods — techniques the papers use, named apart from their topics

kernel association test · 0.6diffusion kernel · 0.6
YearPublicationVenuePosition
2022 Gene set analysis with graph-embedded kernel association test
abstract
MOTIVATION: Kernel-based association test (KAT) has been a popular approach to evaluate the association of expressions of a gene set (e.g. pathway) with a phenotypic trait. KATs rely on kernel functions which capture the sample similarity across multiple features, to capture potential linear or non-linear relationship among features in a gene set. When calculating the kernel functions, no network graphical information about the features is considered. While genes in a functional group (e.g. a pathway) are not independent in general due to regulatory interactions, incorporating regulatory network (or graph) information can potentially increase the power of KAT. In this work, we propose a graph-embedded kernel association test, termed gKAT. gKAT incorporates prior pathway knowledge when constructing a kernel function into hypothesis testing. RESULTS: We apply a diffusion kernel to capture any graph structures in a gene set, then incorporate such information to build a kernel function for further association test. We illustrate the geometric meaning of the approach. Through extensive simulation studies, we show that the proposed gKAT algorithm can improve testing power compared to the one without considering graph structures. Application to a real dataset further demonstrate the utility of the method. AVAILABILITY AND IMPLEMENTATION: The R code used for the analysis can be accessed at https://github.com/JialinQu/gKAT. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Jialin Qu, Yuehua Cui
Bioinform.1