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Simon Fontaine

dblp:270/9382 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2024
0000-0003-1835-1231ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021

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 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › computational microbiology › microbiome analysis
differential abundance testing
0.812024
ADAPT: Analysis of Microbiome Differential Abundance by Pooling Tobit Models · Bioinform. 2024
Bioinformatics and computational biology › computational microbiology
microbiome analysis
0.812024
ADAPT: Analysis of Microbiome Differential Abundance by Pooling Tobit Models · Bioinform. 2024

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

tobit model · 0.8left-censored observation modeling · 0.8
YearPublicationVenuePosition
2024 ADAPT: Analysis of Microbiome Differential Abundance by Pooling Tobit Models
abstract
MOTIVATION: Microbiome differential abundance analysis (DAA) remains a challenging problem despite multiple methods proposed in the literature. The excessive zeros and compositionality of metagenomics data are two main challenges for DAA. RESULTS: We propose a novel method called "Analysis of Microbiome Differential Abundance by Pooling Tobit Models" (ADAPT) to overcome these two challenges. ADAPT interprets zero counts as left-censored observations to avoid unfounded assumptions and complex models. ADAPT also encompasses a theoretically justified way of selecting non-differentially abundant microbiome taxa as a reference to reveal differentially abundant taxa while avoiding false discoveries. We generate synthetic data using independent simulation frameworks to show that ADAPT has more consistent false discovery rate control and higher statistical power than competitors. We use ADAPT to analyze 16S rRNA sequencing of saliva samples and shotgun metagenomics sequencing of plaque samples collected from infants in the COHRA2 study. The results provide novel insights into the association between the oral microbiome and early childhood dental caries. AVAILABILITY AND IMPLEMENTATION: The R package ADAPT can be installed from Bioconductor at https://bioconductor.org/packages/release/bioc/html/ADAPT.html or from Github at https://github.com/mkbwang/ADAPT. The source codes for simulation studies and real data analysis are available at https://github.com/mkbwang/ADAPT_example.
Mukai Wang, Simon Fontaine, Hui Jiang 0002, Gen Li 0004
Bioinform.2