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Jiaxuan Wangwu

dblp:305/6311 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2021
0000-0001-7924-4486ORCID · reported

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 › single-cell analysis › single-cell data integration
single-cell multi-omics integration
0.512021
scAMACE: model-based approach to the joint analysis of single-cell data on chromatin accessibility, gene expression and methylation · Bioinform. 2021
Bioinformatics and computational biology › epigenomics
chromatin accessibility
0.112021
scAMACE: model-based approach to the joint analysis of single-cell data on chromatin accessibility, gene expression and methylation · Bioinform. 2021
Bioinformatics and computational biology
single-cell analysis
0.112021
scAMACE: model-based approach to the joint analysis of single-cell data on chromatin accessibility, gene expression and methylation · Bioinform. 2021

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

expectation-maximization · 0.5GPU implementation · 0.5
YearPublicationVenuePosition
2021 scAMACE: model-based approach to the joint analysis of single-cell data on chromatin accessibility, gene expression and methylation
abstract
MOTIVATION: The advancement in technologies and the growth of available single-cell datasets motivate integrative analysis of multiple single-cell genomic datasets. Integrative analysis of multimodal single-cell datasets combines complementary information offered by single-omic datasets and can offer deeper insights on complex biological process. Clustering methods that identify the unknown cell types are among the first few steps in the analysis of single-cell datasets, and they are important for downstream analysis built upon the identified cell types. RESULTS: We propose scAMACE for the integrative analysis and clustering of single-cell data on chromatin accessibility, gene expression and methylation. We demonstrate that cell types are better identified and characterized through analyzing the three data types jointly. We develop an efficient Expectation-Maximization algorithm to perform statistical inference, and evaluate our methods on both simulation study and real data applications. We also provide the GPU implementation of scAMACE, making it scalable to large datasets. AVAILABILITY AND IMPLEMENTATION: The software and datasets are available at https://github.com/cuhklinlab/scAMACE_py (python implementation) and https://github.com/cuhklinlab/scAMACE (R implementation). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Jiaxuan Wangwu, Zexuan Sun, Zhixiang Lin
Bioinform.1