Demo Data from EDBT 2026 / reviewers in the wild / expert
Priit Adler
dblp:07/3715
· DBLP profile ↗
4ranked-venue papers
1as first author
0since 2021 · last 2020
0000-0001-8276-5135ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 4 · 1 first-author
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
3 papers |
Bioinformatics and computational biology · 83% Computational science and engineering · 17% |
Topics — the 6 heaviest of 7, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › genomics › computational genomics
gene prioritization |
0.2 | 1 | 2015 | FUN-L: gene prioritization for RNAi screens · Bioinform. 2015 |
Bioinformatics and computational biology › functional genomics
RNAi screen analysis |
0.2 | 1 | 2015 | FUN-L: gene prioritization for RNAi screens · Bioinform. 2015 |
Computational science and engineering › information retrieval
rank aggregation |
0.1 | 1 | 2012 | Robust rank aggregation for gene list integration and meta-analysis · Bioinform. 2012 |
Bioinformatics and computational biology
gene expression analysis |
0.1 | 1 | 2008 | KEGGanim: pathway animations for high-throughput data · Bioinform. 2008 |
Bioinformatics and computational biology › systems bioinformatics
pathway analysis |
0.1 | 1 | 2008 | KEGGanim: pathway animations for high-throughput data · Bioinform. 2008 |
Bioinformatics and computational biology › systems bioinformatics › pathway analysis
pathway visualization |
0.1 | 1 | 2008 | KEGGanim: pathway animations for high-throughput data · Bioinform. 2008 |
Methods — techniques the papers use, named apart from their topics
data mining · 0.2data integration · 0.2significance scoring · 0.1probabilistic model · 0.1pathway animation · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2020 | PAWER: protein array web exploreRabstractBACKGROUND: Protein microarray is a well-established approach for characterizing activity levels of thousands of proteins in a parallel manner. Analysis of protein microarray data is complex and time-consuming, while existing solutions are either outdated or challenging to use without programming skills. The typical data analysis pipeline consists of a data preprocessing step, followed by differential expression analysis, which is then put into context via functional enrichment. Normally, biologists would need to assemble their own workflow by combining a set of unrelated tools to analyze experimental data. Provided that most of these tools are developed independently by various bioinformatics groups, making them work together could be a real challenge. RESULTS: Here we present PAWER, the online web tool dedicated solely to protein microarray analysis. PAWER enables biologists to carry out all the necessary analysis steps in one go. PAWER provides access to state-of-the-art computational methods through the user-friendly interface, resulting in publication-ready illustrations. We also provide an R package for more advanced use cases, such as bespoke analysis workflows. CONCLUSIONS: PAWER is freely available at https://biit.cs.ut.ee/pawer . Dmytro Fishman, Ivan Kuzmin, Priit Adler, Jaak Vilo, Hedi Peterson |
BMC Bioinform. | 3 |
| 2015 | FUN-L: gene prioritization for RNAi screensabstractMOTIVATION: Most biological processes remain only partially characterized with many components still to be identified. Given that a whole genome can usually not be tested in a functional assay, identifying the genes most likely to be of interest is of critical importance to avoid wasting resources. RESULTS: Given a set of known functionally related genes and using a state-of-the-art approach to data integration and mining, our Functional Lists (FUN-L) method provides a ranked list of candidate genes for testing. Validation of predictions from FUN-L with independent RNAi screens confirms that FUN-L-produced lists are enriched in genes with the expected phenotypes. In this article, we describe a website front end to FUN-L. AVAILABILITY AND IMPLEMENTATION: The website is freely available to use at http://funl.org Jonathan G. Lees, Jean-Karim Hériché, Ian Morilla, José María Fernández 0001, Priit Adler, Martin Krallinger, Jaak Vilo, Alfonso Valencia, Jan Ellenberg, Juan Garcia Ranea, Christine A. Orengo |
Bioinform. | 5 |
| 2012 | Robust rank aggregation for gene list integration and meta-analysisabstractMOTIVATION: The continued progress in developing technological platforms, availability of many published experimental datasets, as well as different statistical methods to analyze those data have allowed approaching the same research question using various methods simultaneously. To get the best out of all these alternatives, we need to integrate their results in an unbiased manner. Prioritized gene lists are a common result presentation method in genomic data analysis applications. Thus, the rank aggregation methods can become a useful and general solution for the integration task. RESULTS: Standard rank aggregation methods are often ill-suited for biological settings where the gene lists are inherently noisy. As a remedy, we propose a novel robust rank aggregation (RRA) method. Our method detects genes that are ranked consistently better than expected under null hypothesis of uncorrelated inputs and assigns a significance score for each gene. The underlying probabilistic model makes the algorithm parameter free and robust to outliers, noise and errors. Significance scores also provide a rigorous way to keep only the statistically relevant genes in the final list. These properties make our approach robust and compelling for many settings. AVAILABILITY: All the methods are implemented as a GNU R package RobustRankAggreg, freely available at the Comprehensive R Archive Network http://cran.r-project.org/. Raivo Kolde, Sven Laur, Priit Adler, Jaak Vilo |
Bioinform. | 3 |
| 2008 | KEGGanim: pathway animations for high-throughput dataabstractMOTIVATION: Gene expression analysis with microarrays has become one of the most widely used high-throughput methods for gathering genome-wide functional data. Emerging -omics fields such as proteomics and interactomics introduce new information sources. With the rise of systems biology, researchers need to concentrate on entire complex pathways that guide individual genes and related processes. Bioinformatics methods are needed to link the existing knowledge about pathways with the growing amounts of experimental data. RESULTS: We present KEGGanim, a novel web-based tool for visualizing experimental data in biological pathways. KEGGanim produces animations and images of KEGG pathways using public or user uploaded high-throughput data. Pathway members are coloured according to experimental measurements, and animated over experimental conditions. KEGGanim visualization highlights dynamic changes over conditions and allows the user to observe important modules and key genes that influence the pathway. The simple user interface of KEGGanim provides options for filtering genes and experimental conditions. KEGGanim may be used with public or private data for 14 organisms with a large collection of public microarray data readily available. Most common gene and protein identifiers and microarray probesets are accepted for visualization input. AVAILABILITY: http://biit.cs.ut.ee/KEGGanim/. Priit Adler, Jüri Reimand, Jürgen Jänes, Raivo Kolde, Hedi Peterson, Jaak Vilo |
Bioinform. | 1 |