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PHACTboost: A Phylogeny-Aware Pathogenicity Predictor for Missense Mutations via Boosting.
Dereli, Onur; Kuru, Nurdan; Akkoyun, Emrah; Bircan, Aylin; Tastan, Oznur; Adebali, Ogün.
  • Dereli O; Faculty of Engineering and Natural Sciences, Sabanci University, Istanbul 34956, Turkey.
  • Kuru N; Faculty of Engineering and Natural Sciences, Sabanci University, Istanbul 34956, Turkey.
  • Akkoyun E; Faculty of Engineering and Natural Sciences, Sabanci University, Istanbul 34956, Turkey.
  • Bircan A; Network Technologies Department, TÜBITAK-ULAKBIM Turkish Academic Network and Information Center, Ankara 06530, Turkey.
  • Tastan O; Faculty of Engineering and Natural Sciences, Sabanci University, Istanbul 34956, Turkey.
  • Adebali O; Faculty of Engineering and Natural Sciences, Sabanci University, Istanbul 34956, Turkey.
Mol Biol Evol ; 41(7)2024 Jul 03.
Article en En | MEDLINE | ID: mdl-38934805
ABSTRACT
Most algorithms that are used to predict the effects of variants rely on evolutionary conservation. However, a majority of such techniques compute evolutionary conservation by solely using the alignment of multiple sequences while overlooking the evolutionary context of substitution events. We had introduced PHACT, a scoring-based pathogenicity predictor for missense mutations that can leverage phylogenetic trees, in our previous study. By building on this foundation, we now propose PHACTboost, a gradient boosting tree-based classifier that combines PHACT scores with information from multiple sequence alignments, phylogenetic trees, and ancestral reconstruction. By learning from data, PHACTboost outperforms PHACT. Furthermore, the results of comprehensive experiments on carefully constructed sets of variants demonstrated that PHACTboost can outperform 40 prevalent pathogenicity predictors reported in the dbNSFP, including conventional tools, metapredictors, and deep learning-based approaches as well as more recent tools such as AlphaMissense, EVE, and CPT-1. The superiority of PHACTboost over these methods was particularly evident in case of hard variants for which different pathogenicity predictors offered conflicting results. We provide predictions of 215 million amino acid alterations over 20,191 proteins. PHACTboost is available at https//github.com/CompGenomeLab/PHACTboost. PHACTboost can improve our understanding of genetic diseases and facilitate more accurate diagnoses.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Filogenia / Mutación Missense Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Filogenia / Mutación Missense Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article