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Pierre-Aurélien Gilliot

dblp:370/5557 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2023
—ORCID · unresolved

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

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 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 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
massively parallel reporter assay
0.712023
Effective design and inference for cell sorting and sequencing based massively parallel reporter assays · Bioinform. 2023
Bioinformatics and computational biology › statistical genetics
genotype-phenotype prediction
0.212023
Effective design and inference for cell sorting and sequencing based massively parallel reporter assays · Bioinform. 2023

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

simulation · 0.7maximum likelihood estimation · 0.7deep learning · 0.7
YearPublicationVenuePosition
2023 Effective design and inference for cell sorting and sequencing based massively parallel reporter assays
abstract
MOTIVATION: The ability to measure the phenotype of millions of different genetic designs using Massively Parallel Reporter Assays (MPRAs) has revolutionized our understanding of genotype-to-phenotype relationships and opened avenues for data-centric approaches to biological design. However, our knowledge of how best to design these costly experiments and the effect that our choices have on the quality of the data produced is lacking. RESULTS: In this article, we tackle the issues of data quality and experimental design by developing FORECAST, a Python package that supports the accurate simulation of cell-sorting and sequencing-based MPRAs and robust maximum likelihood-based inference of genetic design function from MPRA data. We use FORECAST's capabilities to reveal rules for MPRA experimental design that help ensure accurate genotype-to-phenotype links and show how the simulation of MPRA experiments can help us better understand the limits of prediction accuracy when this data are used for training deep learning-based classifiers. As the scale and scope of MPRAs grows, tools like FORECAST will help ensure we make informed decisions during their development and the most of the data produced. AVAILABILITY AND IMPLEMENTATION: The FORECAST package is available at: https://gitlab.com/Pierre-Aurelien/forecast. Code for the deep learning analysis performed in this study is available at: https://gitlab.com/Pierre-Aurelien/rebeca.
Pierre-Aurélien Gilliot, Thomas E. Gorochowski
Bioinform.1