Learning-based fault localization has been intensively studied recently. Prior studies have shown that traditional Learning-to-Rank techniques can help precisely diagnose fault locations using various dimensions of fault-diagnosis features, such as suspiciousness values computed by various off-the-shelf fault localization techniques. However, with the increasing dimensions of features considered by advanced fault localization techniques, it can be quite challenging for the traditional Learning-to-Rank algorithms to automatically identify effective existing/latent features. In this work, we propose DeepFL, a deep learning approach to automatically learn the most effective existing/latent features for precise fault localization. Although the approach is general, in this work, we collect various suspiciousness-value-based, fault-proneness-based and textual-similarity-based features from the fault localization, defect prediction and information retrieval areas, respectively. DeepFL has been studied on 395 real bugs from the widely used Defects4J benchmark. The experimental results show DeepFL can significantly outperform state-of-the-art TraPT/FLUCCS (e.g., localizing 50+ more faults within Top-1). We also investigate the impacts of deep model configurations (e.g., loss functions and epoch settings) and features. Furthermore, DeepFL is also surprisingly effective for cross-project prediction.
Deep Just-in-Time Defect Prediction: How Far Are We?
Defect prediction aims to automatically identify potential defective code with minimal human intervention and has been widely studied in the literature. Just-in-Time (JIT) defect prediction focuses on program changes rather than whole programs, and has been widely adopted in continuous testing. CC2Vec, state-of-the-art JIT defect prediction tool, first constructs a hierarchical attention network (HAN) to learn distributed vector representations of both code additions and deletions, and then concatenates them with two other embedding vectors representing commit messages and overall code changes extracted by the existing DeepJIT approach to train a model for predicting whether a given commit is defective. Although CC2Vec has been shown to be the state of the art for JIT defect prediction, it was only evaluated on a limited dataset and not compared with all representative baselines. Therefore, to further investigate the efficacy and limitations of CC2Vec, this paper performs an extensive study of CC2Vec on a large-scale dataset with over 310,370 changes (8.3 X larger than the original CC2Vec dataset). More specifically, we also empirically compare CC2Vec against DeepJIT and representative traditional JIT defect prediction techniques. The experimental results show that CC2Vec cannot consistently outperform DeepJIT, and neither of them can consistently outperform traditional JIT defect more »
- Publication Date:
- NSF-PAR ID:
- 10273272
- Journal Name:
- ACM SIGSOFT International Symposium on Software Testing and Analysis
- Sponsoring Org:
- National Science Foundation
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Build systems are essential for modern software development and maintenance since they are widely used to transform source code artifacts into executable software. Previous work shows that build systems break frequently during software evolution. Therefore, automated build-fixing techniques are in huge demand. In this paper we target a mainstream build system, Gradle, which has become the most widely used build system for Java projects in the open-source community (e.g., GitHub). HireBuild, state-of-the-art build-fixing tool for Gradle, has been recently proposed to fix Gradle build failures via mining the history of prior fixes. Although HireBuild has been shown to be effective for fixing real-world Gradle build failures, it was evaluated on only a limited set of build failures, and largely depends on the quality/availability of historical fix information. To investigate the efficacy and limitations of the history-driven build fix, we first construct a new and large build failure dataset from Top-1000 GitHub projects. Then, we evaluate HireBuild on the extended dataset both quantitatively and qualitatively. Inspired by the findings of the study, we propose a simplistic new technique that generates potential patches via searching from the present project under test and external resources rather than the historical fix information. According tomore »
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Abstract Background Drug sensitivity prediction and drug responsive biomarker selection on high-throughput genomic data is a critical step in drug discovery. Many computational methods have been developed to serve this purpose including several deep neural network models. However, the modular relations among genomic features have been largely ignored in these methods. To overcome this limitation, the role of the gene co-expression network on drug sensitivity prediction is investigated in this study. Methods In this paper, we first introduce a network-based method to identify representative features for drug response prediction by using the gene co-expression network. Then, two graph-based neural network models are proposed and both models integrate gene network information directly into neural network for outcome prediction. Next, we present a large-scale comparative study among the proposed network-based methods, canonical prediction algorithms (i.e., Elastic Net, Random Forest, Partial Least Squares Regression, and Support Vector Regression), and deep neural network models for drug sensitivity prediction. All the source code and processed datasets in this study are available at https://github.com/compbiolabucf/drug-sensitivity-prediction . Results In the comparison of different feature selection methods and prediction methods on a non-small cell lung cancer (NSCLC) cell line RNA-seq gene expression dataset with 50 different drug treatments, wemore »
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Concurrent programs are difficult to test due to their inherent non-determinism. To address this problem, testing often requires the exploration of thread schedules of a program; this can be time-consuming when applied to real-world programs. Software defect prediction has been used to help developers find faults and prioritize their testing efforts. Prior studies have used machine learning to build such predicting models based on designed features that encode the characteristics of programs. However, research has focused on sequential programs; to date, no work has considered defect prediction for concurrent programs, with program characteristics distinguished from sequential programs. In this paper, we present ConPredictor, an approach to predict defects specific to concurrent programs by combining both static and dynamic program metrics. Specifically, we propose a set of novel static code metrics based on the unique properties of concurrent programs. We also leverage additional guidance from dynamic metrics constructed based on mutation analysis. Our evaluation on four large open source projects shows that ConPredictor improved both within-project defect prediction and cross-project defect prediction compared to traditional features.
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Results We develop EnQA, a novel graph-based 3D-equivariant neural network method that is equivariant to rotation and translation of 3D objects to estimate the accuracy of protein structural models by leveraging the structural features acquired from the state-of-the-art tertiary structure prediction method—AlphaFold2. We train and test the method on both traditional model datasets (e.g. the datasets of the Critical Assessment of Techniques for Protein Structure Prediction) and a new dataset of high-quality structural models predicted only by AlphaFold2 for the proteins whose experimental structures were released recently. Our approach achieves state-of-the-art performance on protein structural models predicted by both traditional protein structure prediction methods and the latest end-to-end deep learning method—AlphaFold2. It performs even better than the model QA scores provided by AlphaFold2 itself.more »
Availability and implementation The source code is available at https://github.com/BioinfoMachineLearning/EnQA.
Supplementary information Supplementary data are available at Bioinformatics online.
- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Publisher's Version of Record
- https://doi.org/10.1145/3460319.3464819
