Demo Data from EDBT 2026 / reviewers in the wild / expert
Michael F. Adamer
dblp:203/8407
· DBLP profile ↗
2ranked-venue papers
2as first author
2since 2021 · last 2024
0000-0002-8996-7167ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2 · 2 first-author · 2 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
2 papers |
Bioinformatics and computational biology · 100% |
Topics — the 4 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
biomarker discovery |
0.8 | 1 | 2024 | Biomarker identification by interpretable maximum mean discrepancy · Bioinform. 2024 |
Bioinformatics and computational biology
feature selection |
0.8 | 1 | 2024 | Biomarker identification by interpretable maximum mean discrepancy · Bioinform. 2024 |
Bioinformatics and computational biology › biostatistics › statistical bioinformatics
statistical genomics |
0.8 | 1 | 2024 | Biomarker identification by interpretable maximum mean discrepancy · Bioinform. 2024 |
Bioinformatics and computational biology › sequence analysis
similarity search |
0.7 | 1 | 2023 | SIMBSIG: similarity search and clustering for biobank-scale data · Bioinform. 2023 |
Methods — techniques the papers use, named apart from their topics
sparse optimization · 0.8shapley additive explanations · 0.8maximum mean discrepancy · 0.8principal component analysis · 0.7out-of-core computation · 0.7GPU computing · 0.7
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2024 | Biomarker identification by interpretable maximum mean discrepancyabstractMOTIVATION: In many biomedical applications, we are confronted with paired groups of samples, such as treated versus control. The aim is to detect discriminating features, i.e. biomarkers, based on high-dimensional (omics-) data. This problem can be phrased more generally as a two-sample problem requiring statistical significance testing to establish differences, and interpretations to identify distinguishing features. The multivariate maximum mean discrepancy (MMD) test quantifies group-level differences, whereas statistically significantly associated features are usually found by univariate feature selection. Currently, few general-purpose methods simultaneously perform multivariate feature selection and two-sample testing. RESULTS: We introduce a sparse, interpretable, and optimized MMD test (SpInOpt-MMD) that enables two-sample testing and feature selection in the same experiment. SpInOpt-MMD is a versatile method and we demonstrate its application to a variety of synthetic and real-world data types including images, gene expression measurements, and text data. SpInOpt-MMD is effective in identifying relevant features in small sample sizes and outperforms other feature selection methods such as SHapley Additive exPlanations and univariate association analysis in several experiments. AVAILABILITY AND IMPLEMENTATION: The code and links to our public data are available at https://github.com/BorgwardtLab/spinoptmmd. Michael F. Adamer, Sarah C. Brüningk, Dexiong Chen, Karsten M. Borgwardt |
Bioinform. | 1 |
| 2023 | SIMBSIG: similarity search and clustering for biobank-scale dataabstractSUMMARY: In many modern bioinformatics applications, such as statistical genetics, or single-cell analysis, one frequently encounters datasets which are orders of magnitude too large for conventional in-memory analysis. To tackle this challenge, we introduce SIMBSIG (SIMmilarity Batched Search Integrated GPU), a highly scalable Python package which provides a scikit-learn-like interface for out-of-core, GPU-enabled similarity searches, principal component analysis and clustering. Due to the PyTorch backend, it is highly modular and particularly tailored to many data types with a particular focus on biobank data analysis. AVAILABILITY AND IMPLEMENTATION: SIMBSIG is freely available from PyPI and its source code and documentation can be found on GitHub (https://github.com/BorgwardtLab/simbsig) under a BSD-3 license. Michael F. Adamer, Eljas Roellin, Lucie Bourguignon, Karsten M. Borgwardt |
Bioinform. | 1 |