APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants

Salvatore Daniele Bianco, Luca Parca, Francesco Petrizzelli, Tommaso Biagini, Agnese Giovannetti, Niccolò Liorni, Alessandro Napoli, Massimo Carella et al.

Nature Communications 2023 article cited by 42

importance 5/10 ai assisted Genomics and Rare Diseases clinical genetics stage: research

Interpreting the pathogenicity of missense variants in mitochondrial DNA is difficult due to highly variable clinical manifestations.

Misclassified mitochondrial variants can delay or misdirect diagnosis of mitochondrial disorders.

APOGEE 2, an improved ensemble machine-learning method with a curated training set, predicts pathogenicity of mitochondrial missense variants and provides region-wise genome fragility assessments.

'Enhanced performance metrics' claimed; no concrete numbers stated

Precompiled APOGEE 2 scores and probabilities made available for clinical and research use.

Venue Nature Communications
Published 2023
Work type article
Authors Salvatore Daniele Bianco, Luca Parca, Francesco Petrizzelli, Tommaso Biagini, Agnese Giovannetti, Niccolò Liorni, Alessandro Napoli, Massimo Carella et al.
Citations 42 (OpenAlex, at import time)
References 54
Model or method APOGEE 2 (ensemble machine-learning method)
Organization not stated in source
Primary source https://doi.org/10.1038/s41467-023-40797-7
Open access gold
Keywords mitochondrial DNA, missense variants, pathogenicity, machine learning, ensemble
5 / 10

real but narrower advance

Variant interpretation for mitochondrial disorders is a real clinical need, but abstract gives no scale or prevalence; a useful diagnostic tool for a specific genetic domain.

Basis: inferred. Judged from the source text, which gives no explicit scale. Stated scale: not stated in source. Method and limits.

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