Evolutionary computation, machine learning and data mining in bioinformatics. EvoBIO (Conference)最新文献

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Optimal Use of Biological Expert Knowledge from Literature Mining in Ant Colony Optimization for Analysis of Epistasis in Human Disease 基于文献挖掘的生物专家知识在人类疾病上位分析中的蚁群优化应用
Arvis Sulovari, Jeff Kiralis, J. Moore
{"title":"Optimal Use of Biological Expert Knowledge from Literature Mining in Ant Colony Optimization for Analysis of Epistasis in Human Disease","authors":"Arvis Sulovari, Jeff Kiralis, J. Moore","doi":"10.1007/978-3-642-37189-9_12","DOIUrl":"https://doi.org/10.1007/978-3-642-37189-9_12","url":null,"abstract":"","PeriodicalId":90497,"journal":{"name":"Evolutionary computation, machine learning and data mining in bioinformatics. EvoBIO (Conference)","volume":"51 1","pages":"129-140"},"PeriodicalIF":0.0,"publicationDate":"2013-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90998261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Hybrid Multiobjective Artificial Bee Colony with Differential Evolution Applied to Motif Finding 差分进化混合多目标人工蜂群在基序查找中的应用
D. L. González-Álvarez, M. A. Vega-Rodríguez
{"title":"Hybrid Multiobjective Artificial Bee Colony with Differential Evolution Applied to Motif Finding","authors":"D. L. González-Álvarez, M. A. Vega-Rodríguez","doi":"10.1007/978-3-642-37189-9_7","DOIUrl":"https://doi.org/10.1007/978-3-642-37189-9_7","url":null,"abstract":"","PeriodicalId":90497,"journal":{"name":"Evolutionary computation, machine learning and data mining in bioinformatics. EvoBIO (Conference)","volume":"53 1","pages":"68-79"},"PeriodicalIF":0.0,"publicationDate":"2013-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91242741","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Improving the Performance of CGPANN for Breast Cancer Diagnosis Using Crossover and Radial Basis Functions 利用交叉和径向基函数提高CGPANN在乳腺癌诊断中的性能
T. Manning, P. Walsh
{"title":"Improving the Performance of CGPANN for Breast Cancer Diagnosis Using Crossover and Radial Basis Functions","authors":"T. Manning, P. Walsh","doi":"10.1007/978-3-642-37189-9_15","DOIUrl":"https://doi.org/10.1007/978-3-642-37189-9_15","url":null,"abstract":"","PeriodicalId":90497,"journal":{"name":"Evolutionary computation, machine learning and data mining in bioinformatics. EvoBIO (Conference)","volume":"124 1","pages":"165-176"},"PeriodicalIF":0.0,"publicationDate":"2013-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80409415","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 13
Dimensionality Reduction via Isomap with Lock-Step and Elastic Measures for Time Series Gene Expression Classification 基于锁步和弹性度量的等距图降维方法在时间序列基因表达分类中的应用
C. Orsenigo, C. Vercellis
{"title":"Dimensionality Reduction via Isomap with Lock-Step and Elastic Measures for Time Series Gene Expression Classification","authors":"C. Orsenigo, C. Vercellis","doi":"10.1007/978-3-642-37189-9_9","DOIUrl":"https://doi.org/10.1007/978-3-642-37189-9_9","url":null,"abstract":"","PeriodicalId":90497,"journal":{"name":"Evolutionary computation, machine learning and data mining in bioinformatics. EvoBIO (Conference)","volume":"36 1","pages":"92-103"},"PeriodicalIF":0.0,"publicationDate":"2013-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80984085","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
ACO-Based Bayesian Network Ensembles for the Hierarchical Classification of Ageing-Related Proteins 基于aco的贝叶斯网络集成在衰老相关蛋白分层分类中的应用
Khalid M. Salama, A. Freitas
{"title":"ACO-Based Bayesian Network Ensembles for the Hierarchical Classification of Ageing-Related Proteins","authors":"Khalid M. Salama, A. Freitas","doi":"10.1007/978-3-642-37189-9_8","DOIUrl":"https://doi.org/10.1007/978-3-642-37189-9_8","url":null,"abstract":"","PeriodicalId":90497,"journal":{"name":"Evolutionary computation, machine learning and data mining in bioinformatics. EvoBIO (Conference)","volume":"19 1","pages":"80-91"},"PeriodicalIF":0.0,"publicationDate":"2013-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81919850","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
Multiple Threshold Spatially Uniform ReliefF for the Genetic Analysis of Complex Human Diseases 用于复杂人类疾病遗传分析的多阈值空间均匀缓解
Delaney Granizo-MacKenzie, J. Moore
{"title":"Multiple Threshold Spatially Uniform ReliefF for the Genetic Analysis of Complex Human Diseases","authors":"Delaney Granizo-MacKenzie, J. Moore","doi":"10.1007/978-3-642-37189-9_1","DOIUrl":"https://doi.org/10.1007/978-3-642-37189-9_1","url":null,"abstract":"","PeriodicalId":90497,"journal":{"name":"Evolutionary computation, machine learning and data mining in bioinformatics. EvoBIO (Conference)","volume":"17 1","pages":"1-10"},"PeriodicalIF":0.0,"publicationDate":"2013-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89711411","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 36
Knowledge-constrained K-medoids Clustering of Regulatory Rare Alleles for Burden Tests. 负荷检测中调控稀有等位基因的知识约束k -媒介聚类。
R Michael Sivley, Alexandra E Fish, William S Bush
{"title":"Knowledge-constrained K-medoids Clustering of Regulatory Rare Alleles for Burden Tests.","authors":"R Michael Sivley,&nbsp;Alexandra E Fish,&nbsp;William S Bush","doi":"10.1007/978-3-642-37189-9_4","DOIUrl":"https://doi.org/10.1007/978-3-642-37189-9_4","url":null,"abstract":"<p><p>Rarely occurring genetic variants are hypothesized to influence human diseases, but statistically associating these rare variants to disease is challenging due to a lack of statistical power in most feasibly sized datasets. Several statistical tests have been developed to either collapse multiple rare variants from a genomic region into a single variable (presence/absence) or to tally the number of rare alleles within a region, relating the burden of rare alleles to disease risk. Both these approaches, however, rely on user-specification of a genomic region to generate these collapsed or burden variables, usually an entire gene. Recent studies indicate that most risk variants for common diseases are found within regulatory regions, not genes. To capture the effect of rare alleles within non-genic regulatory regions for burden tests, we contrast a simple sliding window approach with a knowledge-guided k-medoids clustering method to group rare variants into statistically powerful, biologically meaningful windows. We apply these methods to detect genomic regions that alter expression of nearby genes.</p>","PeriodicalId":90497,"journal":{"name":"Evolutionary computation, machine learning and data mining in bioinformatics. EvoBIO (Conference)","volume":"7833 ","pages":"35-42"},"PeriodicalIF":0.0,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/978-3-642-37189-9_4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32936927","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Biomedical text categorization with concept graph representations using a controlled vocabulary 使用受控词汇表的概念图表示的生物医学文本分类
Meenakshi Mishra, Jun Huan, S. Bleik, Min Song
{"title":"Biomedical text categorization with concept graph representations using a controlled vocabulary","authors":"Meenakshi Mishra, Jun Huan, S. Bleik, Min Song","doi":"10.1145/2350176.2350181","DOIUrl":"https://doi.org/10.1145/2350176.2350181","url":null,"abstract":"Recent work using graph representations for text categorization has shown promising performance over conventional bag-of-words representation of text documents. In this paper we investigate a graph representation of texts for the task of text categorization. In our representation we identify high level concepts extracted from a database of controlled biomedical terms and build a rich graph structure that contains important concepts and relationships. This procedure ensures that graphs are described with a regular vocabulary, leading to increased ease of comparison. We then classify document graphs by applying a set-based graph kernel that is intuitively sensible and able to deal with the disconnectedness of the constructed concept graphs. We compare this approach to standard approaches using non-graph, text-based features. We also do a comparison amongst different kernels that can be used to see which performs better.","PeriodicalId":90497,"journal":{"name":"Evolutionary computation, machine learning and data mining in bioinformatics. EvoBIO (Conference)","volume":"43 1","pages":"26-32"},"PeriodicalIF":0.0,"publicationDate":"2012-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73425854","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 21
Globalized bipartite local model for drug-target interaction prediction 药物-靶标相互作用预测的全球化二部局部模型
Jianxiang Mei, C. Kwoh, Peng Yang, X. Li, Jie Zheng
{"title":"Globalized bipartite local model for drug-target interaction prediction","authors":"Jianxiang Mei, C. Kwoh, Peng Yang, X. Li, Jie Zheng","doi":"10.1145/2350176.2350178","DOIUrl":"https://doi.org/10.1145/2350176.2350178","url":null,"abstract":"In pharmacology, it is essential to identify the interactions between drug and targets to understand its effects. Supervised learning with Bipartite Local Model (BLM) recently has been shown to be effective for prediction of drug-target interactions by first predicting target proteins of a given known drug, then predicting drugs targeting a known protein. However, this pure \"local\" model is inapplicable to new drug or target candidates that currently have no known interactions. In this paper, we extend the existing BLM method by integrating a strategy for handling new drug and target candidates. Based on the assumption that similar drugs and targets have similar interaction profiles, we present a simple neighbor-based training data inferring procedure and integrate it into the frame work of BLM. This globalized BLM called bipartite local model with neighbor-based inferring (BLMN) then has an extended functionality for prediction interactions between new drug candidates and new target candidates. Good performance of BLMN has been observed in the experiment of predicting interactions between drugs and four important categories of targets. For the Nuclear Receptors dataset, where there are more chances for the presented strategy to be applied, 20% improvement in terms of AUPR was achieved. This demonstrates the effectiveness of BLMN and its potential in prediction of drug-target interactions.","PeriodicalId":90497,"journal":{"name":"Evolutionary computation, machine learning and data mining in bioinformatics. EvoBIO (Conference)","volume":"47 1","pages":"8-14"},"PeriodicalIF":0.0,"publicationDate":"2012-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78252135","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
2D similarity kernels for biological sequence classification 生物序列分类的二维相似核
P. Kuksa
{"title":"2D similarity kernels for biological sequence classification","authors":"P. Kuksa","doi":"10.1145/2350176.2350179","DOIUrl":"https://doi.org/10.1145/2350176.2350179","url":null,"abstract":"String kernel-based machine learning methods have yielded great success in practical tasks of structured/sequential data analysis. They often exhibit state-of-the-art performance on tasks such as document topic elucidation, biological sequence classification, or protein superfamily and fold prediction. However, typical string kernel methods rely on analysis of discrete 1D string data (e.g., DNA or amino acid sequences). This work introduces new 2D kernel methods for sequence data in the form of sequences of feature vectors (as in biological sequence profiles, or sequences of individual amino acid physico-chemical descriptors). On three protein sequence classification tasks proposed 2D kernels show significant 15-20% improvements compared to state-of-the-art sequence classification methods.","PeriodicalId":90497,"journal":{"name":"Evolutionary computation, machine learning and data mining in bioinformatics. EvoBIO (Conference)","volume":"1 1","pages":"15-20"},"PeriodicalIF":0.0,"publicationDate":"2012-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86924179","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
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