ArticleBMC bioinformatics2019
Visualizing complex feature interactions and feature sharing in genomic deep neural networks.
Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed.
- Interpreting cis-regulatory interactions from large-scale deep neural networks.Nature genetics · 2024Article
- Designing interpretable deep learning applications for functional genomics: a quantitative analysis.Briefings in bioinformatics · 2024Review
- InterpretingbioRxiv : the preprint server for biology · 2024Article
- NeuronMotif: Deciphering cis-regulatory codes by layer-wise demixing of deep neural networks.Proceedings of the National Academy of Sciences of the United States of America · 2023Article
- MIDRC CRP10 AI interface-an integrated tool for exploring, testing and visualization of AI models.Physics in medicine and biology · 2023Article
- Multinomial Convolutions for Joint Modeling of Regulatory Motifs and Sequence Activity Readouts.Genes · 2022Article
- Neural network modeling of differential binding between wild-type and mutant CTCF reveals putative binding preferences for zinc fingers 1-2.BMC genomics · 2022Article
- A self-attention model for inferring cooperativity between regulatory features.Nucleic acids research · 2021Article
- Global importance analysis: An interpretability method to quantify importance of genomic features in deep neural networks.PLoS computational biology · 2021Article
- Deep neural networks identify sequence context features predictive of transcription factor binding.Nature machine intelligence · 2021Article
- Introspective analysis of convolutional neural networks for improving discrimination performance and feature visualisation.PeerJ. Computer science · 2021Article
- Antibody complementarity determining region design using high-capacity machine learning.Bioinformatics (Oxford, England) · 2020Article
- Deep learning for inferring transcription factor binding sites.Current opinion in systems biology · 2020Article
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Authors and funding
3 authors.
Funding
Abstract
backgroundVisualization tools for deep learning models typically focus on discovering key input features without considering how such low level features are combined in intermediate layers to make decisions. Moreover, many of these methods examine a network's response to specific input examples that may be insufficient to reveal the complexity of model decision making.
resultsWe present DeepResolve, an analysis framework for deep convolutional models of genome function that visualizes how input features contribute individually and combinatorially to network decisions. Unlike other methods, DeepResolve does not depend upon the analysis of a predefined set of inputs. Rather, it uses gradient ascent to stochastically explore intermediate feature maps to 1) discover important features, 2) visualize their contribution and interaction patterns, and 3) analyze feature sharing across tasks that suggests shared biological mechanism. We demonstrate the visualization of decision making using our proposed method on deep neural networks trained on both experimental and synthetic data. DeepResolve is competitive with existing visualization tools in discovering key sequence features, and identifies certain negative features and non-additive feature interactions that are not easily observed with existing tools. It also recovers similarities between poorly correlated classes which are not observed by traditional methods. DeepResolve reveals that DeepSEA's learned decision structure is shared across genome annotations including histone marks, DNase hypersensitivity, and transcription factor binding. We identify groups of TFs that suggest known shared biological mechanism, and recover correlation between DNA hypersensitivities and TF/Chromatin marks.
conclusionsDeepResolve is capable of visualizing complex feature contribution patterns and feature interactions that contribute to decision making in genomic deep convolutional networks. It also recovers feature sharing and class similarities which suggest interesting biological mechanisms. DeepResolve is compatible with existing visualization tools and provides complementary insights.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.