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Nicolas Fourel

dblp:156/9714 · 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 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics
genome visualization
0.212015
GenPlay Multi-Genome, a tool to compare and analyze multiple human genomes in a graphical interface · Bioinform. 2015
Bioinformatics and computational biology › genomics
genomic variant analysis
0.212015
GenPlay Multi-Genome, a tool to compare and analyze multiple human genomes in a graphical interface · Bioinform. 2015
Bioinformatics and computational biology › genomics › genome visualization
structural variant visualization
0.212015
GenPlay Multi-Genome, a tool to compare and analyze multiple human genomes in a graphical interface · Bioinform. 2015
Bioinformatics and computational biology › genomics
personal genomics
0.112015
GenPlay Multi-Genome, a tool to compare and analyze multiple human genomes in a graphical interface · Bioinform. 2015

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

variant calling format parsing · 0.2multi-track visualization · 0.2
YearPublicationVenuePosition
2015 GenPlay Multi-Genome, a tool to compare and analyze multiple human genomes in a graphical interface
abstract
SUMMARY: Parallel visualization of multiple individual human genomes is a complex endeavor that is rapidly gaining importance with the increasing number of personal, phased and cancer genomes that are being generated. It requires the display of variants such as SNPs, indels and structural variants that are unique to specific genomes and the introduction of multiple overlapping gaps in the reference sequence. Here, we describe GenPlay Multi-Genome, an application specifically written to visualize and analyze multiple human genomes in parallel. GenPlay Multi-Genome is ideally suited for the comparison of allele-specific expression and functional genomic data obtained from multiple phased genomes in a graphical interface with access to multiple-track operation. It also allows the analysis of data that have been aligned to custom genomes rather than to a standard reference and can be used as a variant calling format file browser and as a tool to compare different genome assembly, such as hg19 and hg38. AVAILABILITY AND IMPLEMENTATION: GenPlay is available under the GNU public license (GPL-3) from http://genplay.einstein.yu.edu. The source code is available at https://github.com/JulienLajugie/GenPlay.
Julien Lajugie, Nicolas Fourel, Eric E. Bouhassira
Bioinform.2