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Alexandre Fournier-Level

dblp:198/8215 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2017
0000-0002-6047-7164ORCID · reported

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 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics
genome-wide association study
0.312017
GWAlpha: genome-wide estimation of additive effects (alpha) based on trait quantile distribution from pool-sequencing experiments · Bioinform. 2017
Bioinformatics and computational biology › genomics
genomic data analysis
0.312017
GWAlpha: genome-wide estimation of additive effects (alpha) based on trait quantile distribution from pool-sequencing experiments · Bioinform. 2017
Bioinformatics and computational biology › genomics › high-throughput sequencing
pooled sequencing
0.312017
GWAlpha: genome-wide estimation of additive effects (alpha) based on trait quantile distribution from pool-sequencing experiments · Bioinform. 2017

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

quantile distribution modeling · 0.3parametric effect estimation · 0.3
YearPublicationVenuePosition
2017 GWAlpha: genome-wide estimation of additive effects (alpha) based on trait quantile distribution from pool-sequencing experiments
abstract
Motivation: Sequencing pools of individuals (Pool-Seq) is a cost-effective way to gain insight into the genetics of complex traits, but as yet no parametric method has been developed to both test for genetic effects and estimate their magnitude. Here, we propose GWAlpha, a flexible method to obtain parametric estimates of genetic effects genome-wide from Pool-Seq experiments. Results: We showed that GWAlpha powerfully replicates the results of Genome-Wide Association Studies (GWAS) from model organisms. We perform simulation studies that illustrate the effect on power of sample size and number of pools and test the method on different experimental data. Availability and Implementation: GWAlpha is implemented in python, designed to run on Linux operating system and tested on Mac OS. It is freely available at https://github.com/aflevel/GWAlpha . Contact: [email protected]. Supplementary information: Supplementary data are available at Bioinformatics online.
Alexandre Fournier-Level, Charles Robin, David J. Balding
Bioinform.1