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Fredrik J. Swartling

dblp:249/1442 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2019
0000-0002-8460-4367ORCID · reported

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 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › omics data analysis
batch effect correction
0.412019
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
0.412019
Batch-normalization of cerebellar and medulloblastoma gene expression datasets utilizing empirically defined negative control genes · Bioinform. 2019
Bioinformatics and computational biology
gene expression analysis
0.112019
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
YearPublicationVenuePosition
2019 Batch-normalization of cerebellar and medulloblastoma gene expression datasets utilizing empirically defined negative control genes
abstract
MOTIVATION: 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.7