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Incorporating Biological Knowledge with Factor Graph Neural Network for Interpretable Deep Learning

Genomics · Submitted 3 Jun 2019

abstract compiled · 2026-09-23 · no language-model review

The authors' main claim We applied our model to two cancer genomic datasets to predict target clinical variables and achieved better results than other traditional machine learning and deep learning models.

how it is stated · asserted 1.00 read the record →

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arXiv ID1906.00537 (version 1)
Pith IDJZ67CPHM, Pith's permanent record of this paper and its review
CitationAidong Zhang, Tianle Ma. "Incorporating Biological Knowledge with Factor Graph Neural Network for Interpretable Deep Learning." arXiv:1906.00537 (2019). https://pith.science/paper/JZ67CPHM
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Compiled by classifier-1.13.0 via TypeSafe API, question bank abstract-p1-20260923, 2026-09-23: 1 request, 6,804 input tokens.

What the abstract itself states, as probabilities: claims first 0.04 · states limitation 0.08 · human participants 0.43 · controlled comparison 0.37 · randomized assignment 0.01 · states quantitative result 0.06 · compares with prior results 0.94 · mentions code or data availability 0.02.

The abstract, sentence by sentence

arXiv listing abstract v1. Results and the main claim are underlined; .

While deep learning has achieved great success in many fields, one common criticism about deep learning is its lack of interpretability. In most cases, the hidden units in a deep neural network do not have a clear semantic meaning or correspond to any physical entities. However, model interpretability and explainability are crucial in many biomedical applications. To address this challenge, we developed the Factor Graph Neural Network model that is interpretable and predictable by combining probabilistic graphical models with deep learning. We directly encode biological knowledge such as Gene Ontology as a factor graph into the model architecture, making the model transparent and interpretable. Furthermore, we devised an attention mechanism that can capture multi-scale hierarchical interactions among biological entities such as genes and Gene Ontology terms. With parameter sharing mechanism, the unrolled Factor Graph Neural Network model can be trained with stochastic depth and generalize well. We applied our model to two cancer genomic datasets to predict target clinical variables and achieved better results than other traditional machine learning and deep learning models. Our model can also be used for gene set enrichment analysis and selecting Gene Ontology terms that are important to target clinical variables.

background contribution method result interpretation main claim

What the classifier reports for each sentence. The number is the probability it gave the label.
#sentencerolethe authors' own workstates the main conclusionstrength
s0 While deep learning has achieved great success in many fields, one common criticism about deep learning is its lack of interpretability. background 0.99 0.04 0.02 asserted 0.99
s1 In most cases, the hidden units in a deep neural network do not have a clear semantic meaning or correspond to any physical entities. background 0.97 0.06 0.02 asserted 0.96
s2 However, model interpretability and explainability are crucial in many biomedical applications. background 0.93 0.04 0.03 asserted 1.00
s3 To address this challenge, we developed the Factor Graph Neural Network model that is interpretable and predictable by combining probabilistic graphical models with deep learning. contribution 0.69 0.96 0.18 asserted 1.00
s4 We directly encode biological knowledge such as Gene Ontology as a factor graph into the model architecture, making the model transparent and interpretable. method 0.88 0.96 0.11 asserted 1.00
s5 Furthermore, we devised an attention mechanism that can capture multi-scale hierarchical interactions among biological entities such as genes and Gene Ontology terms. method 0.72 0.96 0.05 asserted 0.96
s6 With parameter sharing mechanism, the unrolled Factor Graph Neural Network model can be trained with stochastic depth and generalize well. method 0.97 0.85 0.05 asserted 0.97
s7 We applied our model to two cancer genomic datasets to predict target clinical variables and achieved better results than other traditional machine learning and deep learning models. result 0.99 0.97 0.48 asserted 1.00
s8 Our model can also be used for gene set enrichment analysis and selecting Gene Ontology terms that are important to target clinical variables. contribution 0.70 0.90 0.16 asserted 0.67

What kind of paper the classifier reports this is: method or tool 1.00 · evidence from analysis of existing data 0.82.

What was examined, and what was not

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Every quoted sentence on this record is the authors'. Every label is from Pith's closed vocabulary, with the probability shown beside it. Every number in the measurements table is the authors', checked by code. Record as JSON

The paper
Original abstract

While deep learning has achieved great success in many fields, one common criticism about deep learning is its lack of interpretability. In most cases, the hidden units in a deep neural network do not have a clear semantic meaning or correspond to any physical entities. However, model interpretability and explainability are crucial in many biomedical applications. To address this challenge, we developed the Factor Graph Neural Network model that is interpretable and predictable by combining probabilistic graphical models with deep learning. We directly encode biological knowledge such as Gene Ontology as a factor graph into the model architecture, making the model transparent and interpretable. Furthermore, we devised an attention mechanism that can capture multi-scale hierarchical interactions among biological entities such as genes and Gene Ontology terms. With parameter sharing mechanism, the unrolled Factor Graph Neural Network model can be trained with stochastic depth and generalize well. We applied our model to two cancer genomic datasets to predict target clinical variables and achieved better results than other traditional machine learning and deep learning models. Our model can also be used for gene set enrichment analysis and selecting Gene Ontology terms that are important to target clinical variables.

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References
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5 arXiv papers cite this in 5 sentences

Each citing sentence is taken from the citing paper's LaTeX source and typed by Pith's classifier. A label appears at probability 0.8 or more (0.95 for support), a contest at 0.7 or more; the quoted words are the citing authors'. How each label was checked · JSON

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Compares with 1 paper
  • We compared our methods with traditional machine learning methods Random Forest, Decision Tree and Multilayer Perceptron (MLP), as well as two recent deep learning methods including Graph Convolutional Neural Network (GCN) [ref] , and Prototypical Network [ref] .

    Semi-Supervised Classification with Graph Convolutional Networks · Data preprocessing · 0.98

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