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Ines Colmegna

dblp:177/0010 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2016
—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
epigenomics
0.212016
funtooNorm: an R package for normalization of DNA methylation data when there are multiple cell or tissue types · Bioinform. 2016
Bioinformatics and computational biology › gene expression analysis
microarray data analysis
0.112016
funtooNorm: an R package for normalization of DNA methylation data when there are multiple cell or tissue types · Bioinform. 2016

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

functional normalization · 0.2cross-validation · 0.2
YearPublicationVenuePosition
2016 funtooNorm: an R package for normalization of DNA methylation data when there are multiple cell or tissue types
abstract
MOTIVATION: DNA methylation patterns are well known to vary substantially across cell types or tissues. Hence, existing normalization methods may not be optimal if they do not take this into account. We therefore present a new R package for normalization of data from the Illumina Infinium Human Methylation450 BeadChip (Illumina 450 K) built on the concepts in the recently published funNorm method, and introducing cell-type or tissue-type flexibility. RESULTS: funtooNorm is relevant for data sets containing samples from two or more cell or tissue types. A visual display of cross-validated errors informs the choice of the optimal number of components in the normalization. Benefits of cell (tissue)-specific normalization are demonstrated in three data sets. Improvement can be substantial; it is strikingly better on chromosome X, where methylation patterns have unique inter-tissue variability. AVAILABILITY AND IMPLEMENTATION: An R package is available at https://github.com/GreenwoodLab/funtooNorm, and has been submitted to Bioconductor at http://bioconductor.org.
Kathleen Oros Klein, Stepan Grinek, Sasha Bernatsky, Luigi Bouchard, Antonio Ciampi, Ines Colmegna, Jean-Philippe Fortin, Marie-France Hivert, Marie Hudson, Michael S. Kobor, Aurélie Labbe, Julia L. MacIsaac, Michael J. Meaney 0001, Alexander M. Morin, Kieran J. O'Donnell, Tomi Pastinen, Marinus H. Van Ijzendoorn, Gregory Voisin, Celia M. T. Greenwood
Bioinform.6