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Ragnhild Sørum

dblp:33/4546 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2005
—ORCID · none

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 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis › differential expression analysis
differentially expressed gene identification
0.112005
The influence of missing value imputation on detection of differentially expressed genes from microarray data · Bioinform. 2005
Bioinformatics and computational biology › gene expression analysis
microarray data analysis
0.112005
The influence of missing value imputation on detection of differentially expressed genes from microarray data · Bioinform. 2005

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

linear model · 0.1SAM · 0.1KNNimpute · 0.1ANOVA · 0.1
YearPublicationVenuePosition
2005 The influence of missing value imputation on detection of differentially expressed genes from microarray data
abstract
MOTIVATION: Missing values are problematic for the analysis of microarray data. Imputation methods have been compared in terms of the similarity between imputed and true values in simulation experiments and not of their influence on the final analysis. The focus has been on missing at random, while entries are missing also not at random. RESULTS: We investigate the influence of imputation on the detection of differentially expressed genes from cDNA microarray data. We apply ANOVA for microarrays and SAM and look to the differentially expressed genes that are lost because of imputation. We show that this new measure provides useful information that the traditional root mean squared error cannot capture. We also show that the type of missingness matters: imputing 5% missing not at random has the same effect as imputing 10-30% missing at random. We propose a new method for imputation (LinImp), fitting a simple linear model for each channel separately, and compare it with the widely used KNNimpute method. For 10% missing at random, KNNimpute leads to twice as many lost differentially expressed genes as LinImp. AVAILABILITY: The R package for LinImp is available at http://folk.uio.no/idasch/imp.
Ida Scheel, Magne Aldrin, Ingrid Kristine Glad, Ragnhild Sørum, Heidi Lyng, Arnoldo Frigessi
Bioinform.4