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David Ferreiro

dblp:370/1620 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2024
0000-0003-0757-7702ORCID · reported

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
molecular evolution
0.812024
Selection among site-dependent structurally constrained substitution models of protein evolution by approximate Bayesian computation · Bioinform. 2024
Bioinformatics and computational biology
phylogenetics
0.812024
Selection among site-dependent structurally constrained substitution models of protein evolution by approximate Bayesian computation · Bioinform. 2024

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

regression adjustment · 0.8approximate bayesian computation · 0.8
YearPublicationVenuePosition
2024 Selection among site-dependent structurally constrained substitution models of protein evolution by approximate Bayesian computation
abstract
MOTIVATION: The selection among substitution models of molecular evolution is fundamental for obtaining accurate phylogenetic inferences. At the protein level, evolutionary analyses are traditionally based on empirical substitution models but these models make unrealistic assumptions and are being surpassed by structurally constrained substitution (SCS) models. The SCS models often consider site-dependent evolution, a process that provides realism but complicates their implementation into likelihood functions that are commonly used for substitution model selection. RESULTS: We present a method to perform selection among site-dependent SCS models, also among empirical and site-dependent SCS models, based on the approximate Bayesian computation (ABC) approach and its implementation into the computational framework ProteinModelerABC. The framework implements ABC with and without regression adjustments and includes diverse empirical and site-dependent SCS models of protein evolution. Using extensive simulated data, we found that it provides selection among SCS and empirical models with acceptable accuracy. As illustrative examples, we applied the framework to analyze a variety of protein families observing that SCS models fit them better than the corresponding best-fitting empirical substitution models. AVAILABILITY AND IMPLEMENTATION: ProteinModelerABC is freely available from https://github.com/DavidFerreiro/ProteinModelerABC, can run in parallel and includes a graphical user interface. The framework is distributed with detailed documentation and ready-to-use examples.
David Ferreiro, Catarina Branco, Miguel Arenas
Bioinform.1