{"title":"为基因组学中的可解释人工智能生成语义丰富的本地数据集","authors":"Pedro Barbosa, Rosina Savisaar, Alcides Fonseca","doi":"arxiv-2407.02984","DOIUrl":null,"url":null,"abstract":"Black box deep learning models trained on genomic sequences excel at\npredicting the outcomes of different gene regulatory mechanisms. Therefore,\ninterpreting these models may provide novel insights into the underlying\nbiology, supporting downstream biomedical applications. Due to their\ncomplexity, interpretable surrogate models can only be built for local\nexplanations (e.g., a single instance). However, accomplishing this requires\ngenerating a dataset in the neighborhood of the input, which must maintain\nsyntactic similarity to the original data while introducing semantic\nvariability in the model's predictions. This task is challenging due to the\ncomplex sequence-to-function relationship of DNA. We propose using Genetic Programming to generate datasets by evolving\nperturbations in sequences that contribute to their semantic diversity. Our\ncustom, domain-guided individual representation effectively constrains\nsyntactic similarity, and we provide two alternative fitness functions that\npromote diversity with no computational effort. Applied to the RNA splicing\ndomain, our approach quickly achieves good diversity and significantly\noutperforms a random baseline in exploring the search space, as shown by our\nproof-of-concept, short RNA sequence. Furthermore, we assess its\ngeneralizability and demonstrate scalability to larger sequences, resulting in\na $\\approx$30\\% improvement over the baseline.","PeriodicalId":501070,"journal":{"name":"arXiv - QuanBio - Genomics","volume":"16 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Semantically Rich Local Dataset Generation for Explainable AI in Genomics\",\"authors\":\"Pedro Barbosa, Rosina Savisaar, Alcides Fonseca\",\"doi\":\"arxiv-2407.02984\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Black box deep learning models trained on genomic sequences excel at\\npredicting the outcomes of different gene regulatory mechanisms. Therefore,\\ninterpreting these models may provide novel insights into the underlying\\nbiology, supporting downstream biomedical applications. Due to their\\ncomplexity, interpretable surrogate models can only be built for local\\nexplanations (e.g., a single instance). However, accomplishing this requires\\ngenerating a dataset in the neighborhood of the input, which must maintain\\nsyntactic similarity to the original data while introducing semantic\\nvariability in the model's predictions. This task is challenging due to the\\ncomplex sequence-to-function relationship of DNA. We propose using Genetic Programming to generate datasets by evolving\\nperturbations in sequences that contribute to their semantic diversity. Our\\ncustom, domain-guided individual representation effectively constrains\\nsyntactic similarity, and we provide two alternative fitness functions that\\npromote diversity with no computational effort. Applied to the RNA splicing\\ndomain, our approach quickly achieves good diversity and significantly\\noutperforms a random baseline in exploring the search space, as shown by our\\nproof-of-concept, short RNA sequence. Furthermore, we assess its\\ngeneralizability and demonstrate scalability to larger sequences, resulting in\\na $\\\\approx$30\\\\% improvement over the baseline.\",\"PeriodicalId\":501070,\"journal\":{\"name\":\"arXiv - QuanBio - Genomics\",\"volume\":\"16 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-07-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"arXiv - QuanBio - Genomics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/arxiv-2407.02984\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Genomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2407.02984","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
在基因组序列上训练的黑盒深度学习模型擅长预测不同基因调控机制的结果。因此,对这些模型进行解释可以提供对潜在生物学的新见解,从而支持下游的生物医学应用。由于其复杂性,可解释的代用模型只能针对局部解释(如单个实例)建立。然而,要做到这一点,需要在输入数据的邻域生成一个数据集,该数据集必须与原始数据保持句法相似性,同时在模型预测中引入语义可变性。由于 DNA 的序列与功能之间的关系非常复杂,因此这项任务极具挑战性。我们建议使用遗传编程法(Genetic Programming),通过对序列的扰动来生成数据集,从而促进数据集的语义多样性。我们定制的、以领域为导向的个体表示法有效地约束了句法相似性,我们还提供了两种可供选择的适合度函数,它们能在不增加计算工作量的情况下促进多样性。应用于 RNA 剪接领域,我们的方法很快就实现了良好的多样性,并且在探索搜索空间方面明显优于随机基线,正如我们的概念验证短 RNA 序列所显示的那样。此外,我们还评估了它的通用性,并证明了它对更大序列的可扩展性,结果比基线提高了大约30%。
Semantically Rich Local Dataset Generation for Explainable AI in Genomics
Black box deep learning models trained on genomic sequences excel at
predicting the outcomes of different gene regulatory mechanisms. Therefore,
interpreting these models may provide novel insights into the underlying
biology, supporting downstream biomedical applications. Due to their
complexity, interpretable surrogate models can only be built for local
explanations (e.g., a single instance). However, accomplishing this requires
generating a dataset in the neighborhood of the input, which must maintain
syntactic similarity to the original data while introducing semantic
variability in the model's predictions. This task is challenging due to the
complex sequence-to-function relationship of DNA. We propose using Genetic Programming to generate datasets by evolving
perturbations in sequences that contribute to their semantic diversity. Our
custom, domain-guided individual representation effectively constrains
syntactic similarity, and we provide two alternative fitness functions that
promote diversity with no computational effort. Applied to the RNA splicing
domain, our approach quickly achieves good diversity and significantly
outperforms a random baseline in exploring the search space, as shown by our
proof-of-concept, short RNA sequence. Furthermore, we assess its
generalizability and demonstrate scalability to larger sequences, resulting in
a $\approx$30\% improvement over the baseline.