Rachel Jeitziner

dblp:249/1383 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2019
—ORCID · none

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
gene expression analysis
0.412019
Two-Tier Mapper, an unbiased topology-based clustering method for enhanced global gene expression analysis · Bioinform. 2019
Bioinformatics and computational biology
topological data analysis
0.412019
Two-Tier Mapper, an unbiased topology-based clustering method for enhanced global gene expression analysis · Bioinform. 2019

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

topological data analysis · 0.4mapper algorithm · 0.4
YearPublicationVenuePosition
2019 Two-Tier Mapper, an unbiased topology-based clustering method for enhanced global gene expression analysis
abstract
MOTIVATION: Unbiased clustering methods are needed to analyze growing numbers of complex datasets. Currently available clustering methods often depend on parameters that are set by the user, they lack stability, and are not applicable to small datasets. To overcome these shortcomings we used topological data analysis, an emerging field of mathematics that discerns additional feature and discovers hidden insights on datasets and has a wide application range. RESULTS: We have developed a topology-based clustering method called Two-Tier Mapper (TTMap) for enhanced analysis of global gene expression datasets. First, TTMap discerns divergent features in the control group, adjusts for them, and identifies outliers. Second, the deviation of each test sample from the control group in a high-dimensional space is computed, and the test samples are clustered using a new Mapper-based topological algorithm at two levels: a global tier and local tiers. All parameters are either carefully chosen or data-driven, avoiding any user-induced bias. The method is stable, different datasets can be combined for analysis, and significant subgroups can be identified. It outperforms current clustering methods in sensitivity and stability on synthetic and biological datasets, in particular when sample sizes are small; outcome is not affected by removal of control samples, by choice of normalization, or by subselection of data. TTMap is readily applicable to complex, highly variable biological samples and holds promise for personalized medicine. AVAILABILITY AND IMPLEMENTATION: TTMap is supplied as an R package in Bioconductor. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Rachel Jeitziner, Mathieu Carrière, Jacques Rougemont, Steve Oudot, Kathryn Hess, Cathrin Brisken
Bioinform.1