Demo Data from VLDB 2026 / reviewers in the wild / expert
Arthur Yan
dblp:222/4756
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2018
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1
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 2 heaviest of 2, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › gene expression analysis › gene co-expression analysis
co-expression network inference |
0.3 | 1 | 2018 | A new method for constructing tumor specific gene co-expression networks based on samples with tumor purity heterogeneity · Bioinform. 2018 |
Bioinformatics and computational biology
cancer genomics |
0.1 | 1 | 2018 | A new method for constructing tumor specific gene co-expression networks based on samples with tumor purity heterogeneity · Bioinform. 2018 |
Methods — techniques the papers use, named apart from their topics
mixture model · 0.3graphical model · 0.3
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2018 | A new method for constructing tumor specific gene co-expression networks based on samples with tumor purity heterogeneityabstractMotivation: Tumor tissue samples often contain an unknown fraction of stromal cells. This problem is widely known as tumor purity heterogeneity (TPH) was recently recognized as a severe issue in omics studies. Specifically, if TPH is ignored when inferring co-expression networks, edges are likely to be estimated among genes with mean shift between non-tumor- and tumor cells rather than among gene pairs interacting with each other in tumor cells. To address this issue, we propose Tumor Specific Net (TSNet), a new method which constructs tumor-cell specific gene/protein co-expression networks based on gene/protein expression profiles of tumor tissues. TSNet treats the observed expression profile as a mixture of expressions from different cell types and explicitly models tumor purity percentage in each tumor sample. Results: Using extensive synthetic data experiments, we demonstrate that TSNet outperforms a standard graphical model which does not account for TPH. We then apply TSNet to estimate tumor specific gene co-expression networks based on TCGA ovarian cancer RNAseq data. We identify novel co-expression modules and hub structure specific to tumor cells. Availability and implementation: R codes can be found at https://github.com/petraf01/TSNet. Supplementary information: Supplementary data are available at Bioinformatics online. Francesca Petralia, Arthur Yan, Pei Wang 0014 |
Bioinform. | 4 |