Demo Data from EDBT 2026 / reviewers in the wild / expert
Yunha Yeo
dblp:396/6211
· DBLP profile ↗
1ranked-venue papers
0as first author
1since 2021 · last 2024
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Artificial intelligence and machine learning · 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 · 50% Computational science and engineering · 50% | |
| Databases, data mining, and information retrieval
1 paper |
Data integration and cleaning · 100% |
Topics — the 4 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Computational science and engineering › statistical computing
data imputation |
0.8 | 1 | 2024 | Gene-Gene Relationship Modeling Based on Genetic Evidence for Single-Cell RNA-Seq Data Imputation · NeurIPS 2024 |
Bioinformatics and computational biology › single-cell analysis
single-cell RNA sequencing |
0.8 | 1 | 2024 | Gene-Gene Relationship Modeling Based on Genetic Evidence for Single-Cell RNA-Seq Data Imputation · NeurIPS 2024 |
Data integration and cleaning › missing data › missing value imputation
graph-based imputation |
0.8 | 1 | 2024 | Gene-Gene Relationship Modeling Based on Genetic Evidence for Single-Cell RNA-Seq Data Imputation · NeurIPS 2024 |
Data integration and cleaning › missing data
missing value imputation |
0.8 | 1 | 2024 | Gene-Gene Relationship Modeling Based on Genetic Evidence for Single-Cell RNA-Seq Data Imputation · NeurIPS 2024 |
Methods — techniques the papers use, named apart from their topics
standardization · 1.5kNN graph · 0.8k-NN graph · 0.8
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2024 | Gene-Gene Relationship Modeling Based on Genetic Evidence for Single-Cell RNA-Seq Data ImputationabstractSingle-cell RNA sequencing (scRNA-seq) technologies enable the exploration of cellular heterogeneity and facilitate the construction of cell atlases. However, scRNA-seq data often contain a large portion of missing values (false zeros) or noisy values, hindering downstream analyses. To recover these false zeros, propagation-based imputation methods have been proposed using $k$-NN graphs. However they model only associating relationships among genes within a cell, while, according to well-known genetic evidence, there are both associating and dissociating relationships among genes. To apply this genetic evidence to gene-gene relationship modeling, this paper proposes a novel imputation method that newly employs dissociating relationships in addition to associating relationships. Our method constructs a $k$-NN graph to additionally model dissociating relationships via the negation of a given cell-gene matrix. Moreover, our method standardizes the value distribution (mean and variance) of each gene to have standard distributions regardless of the gene. Through extensive experiments, we demonstrate that the proposed method achieves exceptional performance gains over state-of-the-art methods in both cell clustering and gene expression recovery across six scRNA-seq datasets, validating the significance of using complete gene-gene relationships in accordance with genetic evidence. The source code is available at https://github.com/daehoum1/scCR. Daeho Um, Jiwon Yoon 0002, Seong-Jin Ahn 0002, Yunha Yeo |
NeurIPS | 4 |