bioRxivBioinformaticsPreprint
ET-Pfam: Ensemble transfer learning for protein family prediction
Sofia Escudero, Sofia DuarteiD, Rosario VitaleiD, Emilio FenoyiD, Leandro A. BugnoniD, Diego Humberto MiloneiD, Georgina S. StegmayeriD
Abstract
MotivationDue to the rapid growth of sequence generation, which has surpassed the expert curators ability to manually review and annotate them, the computational annotation of proteins remains a significant challenge in bioinformatics nowadays. The Pfam database contains a large collection of proteins that are nowadays annotated with domain families through multiple sequence alignments and profile Hidden Markov models (pHMMs). However, such computational annotation methods have some limitations such as problems for handling large datasets and the fact that multiple sequence alignments are computationally challenging to compute with high accuracy due to the increase in complexity as the number of sequences and lengths grow. Additionally, each HMM is independently obtained for each family missing the opportunity of learning patterns across families, that is from a complete view of all the dataset. As an alternative, some deep learning (DL) models have been recently proposed, nevertheless with simple representations of the inputs and moderate improvements in performance. ResultsIn this work we present ET-Pfam, a novel approach based on transfer learning and ensembles of multiple DL classifiers to predict functional families in the Pfam database. Several base DL models are first trained using learned representations from a protein large language model, with different hyperparameters to increase diversity. Then, the base models are integrated using classical ensemble strategies and novel voting approaches by learning weights for each model and for each Pfam family. Results demonstrate that the proposed ET-Pfam method can consistently diminish classification error rates compared to individual DL models, boosting prediction performance. Among the novel ensemble strategies presented here, the learned weights by family voting achieved the best performance, with the lowest error rate (7.00%), significantly surpassing the best individual base model error (12.91%) and three competitors of the state- of-the-art on the same Pfam dataset. AvailabilityData and source code are available at https://github.com/sinc-lab/ET-Pfam.
- assay: protein sequence
- research focus: protein structure prediction
- approach: deep learning
- approach: statistical model
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Using Deep Learning to Annotate the Protein Universe
Maxwell L. Bileschi, David Belanger, … Lucy J. Colwell·Nature BiotechnologyPeer-reviewed·Feb 21, 2022
- DeepProteomics: Protein family classification using Shallow and Deep Networks
Anu Vazhayil, R Vinayakumar, KP Soman·bioRxiv·Sep 12, 2018
- GNN2Pfam: Integrating protein sequence and structure with graph neural networks for Pfam domain annotation
Emilio Fenoy, Leandro A. Bugnon, … Georgina S. Stegmayer·Journal of Structural BiologyPeer-reviewed·Feb 2, 2026
- What is hidden in the darkness? Deep-learning assisted large-scale protein family curation uncovers novel protein families and folds
J. Durairaj, A. M. Waterhouse, … J. Pereira·bioRxiv·Mar 14, 2023
- Beyond Homology Transfer: Deep Learning for Automated Annotation of Proteins
Mohammad Nauman, Hafeez Ur Rehman, … Alfredo Benso·Journal of Grid ComputingPeer-reviewed·Jul 28, 2018
- Embeddings from deep learning transfer GO annotations beyond homology
Maria Littmann, Michael Heinzinger, … Burkhard Rost·Scientific ReportsPeer-reviewed·Jan 13, 2021