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Wilfrid Richer

dblp:145/8469 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2014
0000-0003-1802-3529ORCID · reported

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%
Computer graphics and multimedia
1 paper
Visualization and visual analytics · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › cancer genomics › copy number analysis
copy number alteration detection
0.212014
SegAnnDB: interactive Web-based genomic segmentation · Bioinform. 2014
Bioinformatics and computational biology › genomics › genome analysis
genome segmentation
0.212014
SegAnnDB: interactive Web-based genomic segmentation · Bioinform. 2014
Visualization and visual analytics › biological data visualization
genome browser
0.212014
SegAnnDB: interactive Web-based genomic segmentation · Bioinform. 2014
Visualization and visual analytics
interactive visualization
0.212014
SegAnnDB: interactive Web-based genomic segmentation · Bioinform. 2014

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

mathematical segmentation model · 0.4computer vision · 0.4
YearPublicationVenuePosition
2014 SegAnnDB: interactive Web-based genomic segmentation
abstract
MOTIVATION: DNA copy number profiles characterize regions of chromosome gains, losses and breakpoints in tumor genomes. Although many models have been proposed to detect these alterations, it is not clear which model is appropriate before visual inspection the signal, noise and models for a particular profile. RESULTS: We propose SegAnnDB, a Web-based computer vision system for genomic segmentation: first, visually inspect the profiles and manually annotate altered regions, then SegAnnDB determines the precise alteration locations using a mathematical model of the data and annotations. SegAnnDB facilitates collaboration between biologists and bioinformaticians, and uses the University of California, Santa Cruz genome browser to visualize copy number alterations alongside known genes. AVAILABILITY AND IMPLEMENTATION: The breakpoints project on INRIA GForge hosts the source code, an Amazon Machine Image can be launched and a demonstration Web site is http://bioviz.rocq.inria.fr.
Toby Hocking, Valentina Boeva, Guillem Rigaill, Gudrun Schleiermacher, Isabelle Janoueix-Lerosey, Olivier Delattre, Wilfrid Richer, Franck Bourdeaut, Miyuki Suguro, Masao Seto, Francis R. Bach, Jean-Philippe Vert
Bioinform.7