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Céline Raulet-Tomkiewicz

dblp:164/0923 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2015
—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 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › bioimage informatics › live cell imaging analysis
cell motility analysis
0.212015
A generic methodological framework for studying single cell motility in high-throughput time-lapse data · Bioinform. 2015
Bioinformatics and computational biology › bioimage informatics
live cell imaging analysis
0.212015
A generic methodological framework for studying single cell motility in high-throughput time-lapse data · Bioinform. 2015
Bioinformatics and computational biology › single-cell analysis
single-cell trajectory analysis
0.212015
A generic methodological framework for studying single cell motility in high-throughput time-lapse data · Bioinform. 2015

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

unsupervised learning · 0.2statistical hit detection · 0.2cell tracking · 0.2
YearPublicationVenuePosition
2015 A generic methodological framework for studying single cell motility in high-throughput time-lapse data
abstract
MOTIVATION: Motility is a fundamental cellular attribute, which plays a major part in processes ranging from embryonic development to metastasis. Traditionally, single cell motility is often studied by live cell imaging. Yet, such studies were so far limited to low throughput. To systematically study cell motility at a large scale, we need robust methods to quantify cell trajectories in live cell imaging data. RESULTS: The primary contribution of this article is to present Motility study Integrated Workflow (MotIW), a generic workflow for the study of single cell motility in high-throughput time-lapse screening data. It is composed of cell tracking, cell trajectory mapping to an original feature space and hit detection according to a new statistical procedure. We show that this workflow is scalable and demonstrates its power by application to simulated data, as well as large-scale live cell imaging data. This application enables the identification of an ontology of cell motility patterns in a fully unsupervised manner. AVAILABILITY AND IMPLEMENTATION: Python code and examples are available online (http://cbio.ensmp.fr/∼aschoenauer/motiw.html)
Alice Schoenauer Sebag, Sandra Plancade, Céline Raulet-Tomkiewicz, Robert Barouki, Jean-Philippe Vert, Thomas Walter 0003
Bioinform.3