Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Håkon Tjelmeland

dblp:80/3690 · DBLP profile ↗
← Back
1ranked-venue papers
0as first author
0since 2021 · last 2008
—ORCID · unresolved

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 › gene expression analysis › microarray data preprocessing
cross-platform normalization
0.112008
Merging two gene-expression studies via cross-platform normalization · Bioinform. 2008
Bioinformatics and computational biology
gene expression analysis
0.112008
Merging two gene-expression studies via cross-platform normalization · Bioinform. 2008
Bioinformatics and computational biology › data integration
microarray data integration
0.012008
Merging two gene-expression studies via cross-platform normalization · Bioinform. 2008

Methods — techniques the papers use, named apart from their topics

validation measure · 0.1linked gene/sample clustering · 0.1
YearPublicationVenuePosition
2008 Merging two gene-expression studies via cross-platform normalization
abstract
MOTIVATION: Gene-expression microarrays are currently being applied in a variety of biomedical applications. This article considers the problem of how to merge datasets arising from different gene-expression studies of a common organism and phenotype. Of particular interest is how to merge data from different technological platforms. RESULTS: The article makes two contributions to the problem. The first is a simple cross-study normalization method, which is based on linked gene/sample clustering of the given datasets. The second is the introduction and description of several general validation measures that can be used to assess and compare cross-study normalization methods. The proposed normalization method is applied to three existing breast cancer datasets, and is compared to several competing normalization methods using the proposed validation measures. AVAILABILITY: The supplementary materials and XPN Matlab code are publicly available at website: https://genome.unc.edu/xpn
Andrey A. Shabalin, Håkon Tjelmeland, Cheng Fan 0006, Charles M. Perou, Andrew B. Nobel
Bioinform.2