Demo Data from EDBT 2026 / reviewers in the wild / expert
Holger Weishaupt
dblp:249/1475
· DBLP profile ↗
1ranked-venue papers
1as first author
0since 2021 · last 2019
—ORCID · unresolved
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1 · 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
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › omics data analysis
batch effect correction |
0.4 | 1 | 2019 | Batch-normalization of cerebellar and medulloblastoma gene expression datasets utilizing empirically defined negative control genes · Bioinform. 2019 |
Bioinformatics and computational biology › multi-omics data integration
gene expression data integration |
0.4 | 1 | 2019 | Batch-normalization of cerebellar and medulloblastoma gene expression datasets utilizing empirically defined negative control genes · Bioinform. 2019 |
Bioinformatics and computational biology
gene expression analysis |
0.1 | 1 | 2019 | Batch-normalization of cerebellar and medulloblastoma gene expression datasets utilizing empirically defined negative control genes · Bioinform. 2019 |
Methods — techniques the papers use, named apart from their topics
removal of unwanted variation · 0.4negative control gene selection · 0.4
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2019 | Batch-normalization of cerebellar and medulloblastoma gene expression datasets utilizing empirically defined negative control genesabstractMOTIVATION: Medulloblastoma (MB) is a brain cancer predominantly arising in children. Roughly 70% of patients are cured today, but survivors often suffer from severe sequelae. MB has been extensively studied by molecular profiling, but often in small and scattered cohorts. To improve cure rates and reduce treatment side effects, accurate integration of such data to increase analytical power will be important, if not essential. RESULTS: We have integrated 23 transcription datasets, spanning 1350 MB and 291 normal brain samples. To remove batch effects, we combined the Removal of Unwanted Variation (RUV) method with a novel pipeline for determining empirical negative control genes and a panel of metrics to evaluate normalization performance. The documented approach enabled the removal of a majority of batch effects, producing a large-scale, integrative dataset of MB and cerebellar expression data. The proposed strategy will be broadly applicable for accurate integration of data and incorporation of normal reference samples for studies of various diseases. We hope that the integrated dataset will improve current research in the field of MB by allowing more large-scale gene expression analyses. AVAILABILITY AND IMPLEMENTATION: The RUV-normalized expression data is available through the Gene Expression Omnibus (GEO; https://www.ncbi.nlm.nih.gov/geo/) and can be accessed via the GSE series number GSE124814. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Holger Weishaupt, Patrik Johansson, Anders Sundström, Zelmina Lubovac, Björn Olsson, Sven Nelander, Fredrik J. Swartling |
Bioinform. | 1 |