Proceedings. IEEE International Conference on Bioinformatics and Biomedicine最新文献

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Deep Convolutional Neural Networks for Detecting Secondary Structures in Protein Density Maps from Cryo-Electron Microscopy. 用于从冷冻电镜蛋白质密度图中检测二级结构的深度卷积神经网络
Proceedings. IEEE International Conference on Bioinformatics and Biomedicine Pub Date : 2016-12-01 Epub Date: 2017-01-19 DOI: 10.1109/BIBM.2016.7822490
Rongjian Li, Dong Si, Tao Zeng, Shuiwang Ji, Jing He
{"title":"Deep Convolutional Neural Networks for Detecting Secondary Structures in Protein Density Maps from Cryo-Electron Microscopy.","authors":"Rongjian Li, Dong Si, Tao Zeng, Shuiwang Ji, Jing He","doi":"10.1109/BIBM.2016.7822490","DOIUrl":"10.1109/BIBM.2016.7822490","url":null,"abstract":"<p><p>The detection of secondary structure of proteins using three dimensional (3D) cryo-electron microscopy (cryo-EM) images is still a challenging task when the spatial resolution of cryo-EM images is at medium level (5-10Å ). Prior researches focused on the usage of local features that may not capture the global information of image objects. In this study, we propose to use deep learning methods to extract high representative global features and then automatically detect secondary structures of proteins. In particular, we build a convolutional neural network (CNN) classifier that predicts the probability of label for every individual voxel in 3D cryo-EM image with respect to the secondary structure elements of proteins such as <i>α</i>-helix, <i>β</i>-sheet and background. To effectively incorporate the 3D spatial information in protein structures, we propose to perform 3D convolutions in the convolutional layers of CNNs. We show that the proposed CNN classifier can outperform existing SVM method on identifying the secondary structure elements of proteins from 3D cryo-EM medium resolution images.</p>","PeriodicalId":74563,"journal":{"name":"Proceedings. IEEE International Conference on Bioinformatics and Biomedicine","volume":"2016 ","pages":"41-46"},"PeriodicalIF":0.0,"publicationDate":"2016-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952046/pdf/nihms874389.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36106213","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: 0
A Multi-Modal Graph-Based Semi-Supervised Pipeline for Predicting Cancer Survival. 基于多模态图的半监督管道预测癌症生存。
Proceedings. IEEE International Conference on Bioinformatics and Biomedicine Pub Date : 2016-12-01 Epub Date: 2017-01-19 DOI: 10.1109/bibm.2016.7822516
Hamid Reza Hassanzadeh, John H Phan, May D Wang
{"title":"A Multi-Modal Graph-Based Semi-Supervised Pipeline for Predicting Cancer Survival.","authors":"Hamid Reza Hassanzadeh,&nbsp;John H Phan,&nbsp;May D Wang","doi":"10.1109/bibm.2016.7822516","DOIUrl":"https://doi.org/10.1109/bibm.2016.7822516","url":null,"abstract":"<p><p>Cancer survival prediction is an active area of research that can help prevent unnecessary therapies and improve patient's quality of life. Gene expression profiling is being widely used in cancer studies to discover informative biomarkers that aid predict different clinical endpoint prediction. We use multiple modalities of data derived from RNA deep-sequencing (RNA-seq) to predict survival of cancer patients. Despite the wealth of information available in expression profiles of cancer tumors, fulfilling the aforementioned objective remains a big challenge, for the most part, due to the paucity of data samples compared to the high dimension of the expression profiles. As such, analysis of transcriptomic data modalities calls for state-of-the-art big-data analytics techniques that can maximally use all the available data to discover the relevant information hidden within a significant amount of noise. In this paper, we propose a pipeline that predicts cancer patients' survival by exploiting the structure of the input (manifold learning) and by leveraging the unlabeled samples using Laplacian support vector machines, a graph-based semi supervised learning (GSSL) paradigm. We show that under certain circumstances, no single modality per se will result in the best accuracy and by fusing different models together via a stacked generalization strategy, we may boost the accuracy synergistically. We apply our approach to two cancer datasets and present promising results. We maintain that a similar pipeline can be used for predictive tasks where labeled samples are expensive to acquire.</p>","PeriodicalId":74563,"journal":{"name":"Proceedings. IEEE International Conference on Bioinformatics and Biomedicine","volume":"2016 ","pages":"184-189"},"PeriodicalIF":0.0,"publicationDate":"2016-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1109/bibm.2016.7822516","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38151657","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: 5
Analysis of Temporal Constraints in Qualitative Eligibility Criteria of Cancer Clinical Studies. 肿瘤临床研究定性资格标准的时间约束分析。
Proceedings. IEEE International Conference on Bioinformatics and Biomedicine Pub Date : 2016-12-01 Epub Date: 2017-01-19 DOI: 10.1109/BIBM.2016.7822607
Zhe He, Zhiwei Chen, Jiang Bian
{"title":"Analysis of Temporal Constraints in Qualitative Eligibility Criteria of Cancer Clinical Studies.","authors":"Zhe He,&nbsp;Zhiwei Chen,&nbsp;Jiang Bian","doi":"10.1109/BIBM.2016.7822607","DOIUrl":"https://doi.org/10.1109/BIBM.2016.7822607","url":null,"abstract":"<p><p>Clinical studies, especially randomized controlled trials, generate gold-standard medical evidence. However, the lack of population representativeness of clinical studies has hampered their generalizability to the real-world population. Overly restrictive qualitative criteria are often applied to exclude patients. In this work, we develop a lexical-pattern-based tool to structure qualitative eligibility criteria with temporal constraints, with which we analyzed over 10,800 cancer clinical studies. Our results showed that restrictive temporal constraints are often applied on qualitative criteria in cancer studies, limiting the generalizability of their results.</p>","PeriodicalId":74563,"journal":{"name":"Proceedings. IEEE International Conference on Bioinformatics and Biomedicine","volume":"2016 ","pages":"717-722"},"PeriodicalIF":0.0,"publicationDate":"2016-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1109/BIBM.2016.7822607","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35676265","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
CHALLENGES IN MATCHING SECONDARY STRUCTURES IN CRYO-EM: AN EXPLORATION. 低温电镜中二级结构匹配的挑战:探索。
Proceedings. IEEE International Conference on Bioinformatics and Biomedicine Pub Date : 2016-12-01 Epub Date: 2017-01-19 DOI: 10.1109/BIBM.2016.7822776
Devin Haslam, Mohammad Zubair, Desh Ranjan, Abhishek Biswas, Jing He
{"title":"CHALLENGES IN MATCHING SECONDARY STRUCTURES IN CRYO-EM: AN EXPLORATION.","authors":"Devin Haslam,&nbsp;Mohammad Zubair,&nbsp;Desh Ranjan,&nbsp;Abhishek Biswas,&nbsp;Jing He","doi":"10.1109/BIBM.2016.7822776","DOIUrl":"https://doi.org/10.1109/BIBM.2016.7822776","url":null,"abstract":"<p><p>Cryo-electron microscopy is a fast emerging biophysical technique for structural determination of large protein complexes. While more atomic structures are being determined using this technique, it is still challenging to derive atomic structures from density maps produced at medium resolution when no suitable templates are available. A critical step in structure determination is how a protein chain threads through the 3-dimensional density map. A dynamic programming method was previously developed to generate <i>K</i> best matches of secondary structures between the density map and its protein sequence using shortest paths in a related weighted graph. We discuss challenges associated with the creation of the weighted graph and explore heuristic methods to solve the problem of matching secondary structures.</p>","PeriodicalId":74563,"journal":{"name":"Proceedings. IEEE International Conference on Bioinformatics and Biomedicine","volume":"2016 ","pages":"1714-1719"},"PeriodicalIF":0.0,"publicationDate":"2016-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1109/BIBM.2016.7822776","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36106214","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
Sparse Canonical Correlation Analysis via Truncated 1-norm with Application to Brain Imaging Genetics. 截断1-范数稀疏典型相关分析及其在脑成像遗传学中的应用。
Proceedings. IEEE International Conference on Bioinformatics and Biomedicine Pub Date : 2016-01-01 Epub Date: 2017-01-19 DOI: 10.1109/BIBM.2016.7822605
Lei Du, Tuo Zhang, Kefei Liu, Xiaohui Yao, Jingwen Yan, Shannon L Risacher, Lei Guo, Andrew J Saykin, Li Shen
{"title":"Sparse Canonical Correlation Analysis via Truncated <i>ℓ</i><sub>1</sub>-norm with Application to Brain Imaging Genetics.","authors":"Lei Du,&nbsp;Tuo Zhang,&nbsp;Kefei Liu,&nbsp;Xiaohui Yao,&nbsp;Jingwen Yan,&nbsp;Shannon L Risacher,&nbsp;Lei Guo,&nbsp;Andrew J Saykin,&nbsp;Li Shen","doi":"10.1109/BIBM.2016.7822605","DOIUrl":"https://doi.org/10.1109/BIBM.2016.7822605","url":null,"abstract":"<p><p>Discovering bi-multivariate associations between genetic markers and neuroimaging quantitative traits is a major task in brain imaging genetics. Sparse Canonical Correlation Analysis (SCCA) is a popular technique in this area for its powerful capability in identifying bi-multivariate relationships coupled with feature selection. The existing SCCA methods impose either the <i>ℓ</i><sub>1</sub>-norm or its variants. The <i>ℓ</i><sub>0</sub>-norm is more desirable, which however remains unexplored since the <i>ℓ</i><sub>0</sub>-norm minimization is NP-hard. In this paper, we impose the truncated <i>ℓ</i><sub>1</sub>-norm to improve the performance of the <i>ℓ</i><sub>1</sub>-norm based SCCA methods. Besides, we propose two efficient optimization algorithms and prove their convergence. The experimental results, compared with two benchmark methods, show that our method identifies better and meaningful canonical loading patterns in both simulated and real imaging genetic analyse.</p>","PeriodicalId":74563,"journal":{"name":"Proceedings. IEEE International Conference on Bioinformatics and Biomedicine","volume":"2016 ","pages":"707-711"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1109/BIBM.2016.7822605","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35426546","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: 7
Human Absorbable MicroRNA Prediction based on an Ensemble Manifold Ranking Model. 基于集成流形排序模型的人可吸收MicroRNA预测。
Proceedings. IEEE International Conference on Bioinformatics and Biomedicine Pub Date : 2015-11-01 Epub Date: 2015-12-17 DOI: 10.1109/BIBM.2015.7359697
Jiang Shu, Kevin Chiang, Dongyu Zhao, Juan Cui
{"title":"Human Absorbable MicroRNA Prediction based on an Ensemble Manifold Ranking Model.","authors":"Jiang Shu,&nbsp;Kevin Chiang,&nbsp;Dongyu Zhao,&nbsp;Juan Cui","doi":"10.1109/BIBM.2015.7359697","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359697","url":null,"abstract":"<p><p>MicroRNAs, a class of short non-coding RNAs, are able to regulate more than half of human genes and affect many fundamental biological processes. It has been long considered synthesized endogenously until very recent discoveries showing that human can absorb exogenous microRNAs from dietary resources. This finding has raised a challenge scientific question: which exogenous microRNAs can be integrated into human circulation and possibly exert functions in human? Here we present a well-designed ensemble manifold ranking model for identifying human absorbable exogenous miRNAs from 14 common dietary species. Specifically, we have analyzed 4,910 dietary microRNAs with 1,120 features derived based on the microRNA sequence and structure. In total, 70 discriminative features were selected to characterize the circulating microRNAs in human and have been used to infer the possibility of a certain exogenous microRNA getting integrated into human circulation. Finally, 461 dietary microRNAs have been identified as transportable exogenous microRNAs. To assess the performance of our ensemble model, we have validated the top predictions through a milk-feeding study. In addition, 26 microRNAs from two virus species were predicted as transportable and have been validated in two external experiments. The results demonstrate the data-driven computational model is highly promising to study transportable microRNAs while bypassing the complex mechanistic details.</p>","PeriodicalId":74563,"journal":{"name":"Proceedings. IEEE International Conference on Bioinformatics and Biomedicine","volume":"2015 ","pages":"295-300"},"PeriodicalIF":0.0,"publicationDate":"2015-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1109/BIBM.2015.7359697","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36655301","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: 3
Deep Learning of Tissue Fate Features in Acute Ischemic Stroke. 急性缺血性脑卒中组织命运特征的深度学习。
Proceedings. IEEE International Conference on Bioinformatics and Biomedicine Pub Date : 2015-11-01 Epub Date: 2015-12-17 DOI: 10.1109/BIBM.2015.7359869
Noah Stier, Nicholas Vincent, David Liebeskind, Fabien Scalzo
{"title":"Deep Learning of Tissue Fate Features in Acute Ischemic Stroke.","authors":"Noah Stier, Nicholas Vincent, David Liebeskind, Fabien Scalzo","doi":"10.1109/BIBM.2015.7359869","DOIUrl":"10.1109/BIBM.2015.7359869","url":null,"abstract":"<p><p>In acute ischemic stroke treatment, prediction of tissue survival outcome plays a fundamental role in the clinical decision-making process, as it can be used to assess the balance of risk vs. possible benefit when considering endovascular clot-retrieval intervention. For the first time, we construct a deep learning model of tissue fate based on randomly sampled local patches from the hypoperfusion (Tmax) feature observed in MRI immediately after symptom onset. We evaluate the model with respect to the ground truth established by an expert neurologist four days after intervention. Experiments on 19 acute stroke patients evaluated the accuracy of the model in predicting tissue fate. Results show the superiority of the proposed regional learning framework versus a single-voxel-based regression model.</p>","PeriodicalId":74563,"journal":{"name":"Proceedings. IEEE International Conference on Bioinformatics and Biomedicine","volume":"2015 ","pages":"1316-1321"},"PeriodicalIF":0.0,"publicationDate":"2015-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1109/BIBM.2015.7359869","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35363448","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: 47
Integration of multimodal RNA-seq data for prediction of kidney cancer survival. 整合多模态RNA-seq数据预测肾癌生存。
Proceedings. IEEE International Conference on Bioinformatics and Biomedicine Pub Date : 2015-11-01 DOI: 10.1109/BIBM.2015.7359913
Matt Schwartzi, Martin Parkl, John H Phanl, May D Wang
{"title":"Integration of multimodal RNA-seq data for prediction of kidney cancer survival.","authors":"Matt Schwartzi,&nbsp;Martin Parkl,&nbsp;John H Phanl,&nbsp;May D Wang","doi":"10.1109/BIBM.2015.7359913","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359913","url":null,"abstract":"<p><p>Kidney cancer is of prominent concern in modern medicine. Predicting patient survival is critical to patient awareness and developing a proper treatment regimens. Previous prediction models built upon molecular feature analysis are limited to just gene expression data. In this study we investigate the difference in predicting five year survival between unimodal and multimodal analysis of RNA-seq data from gene, exon, junction, and isoform modalities. Our preliminary findings report higher predictive accuracy-as measured by area under the ROC curve (AUC)-for multimodal learning when compared to unimodal learning with both support vector machine (SVM) and k-nearest neighbor (KNN) methods. The results of this study justify further research on the use of multimodal RNA-seq data to predict survival for other cancer types using a larger sample size and additional machine learning methods.</p>","PeriodicalId":74563,"journal":{"name":"Proceedings. IEEE International Conference on Bioinformatics and Biomedicine","volume":"2015 ","pages":"1591-1595"},"PeriodicalIF":0.0,"publicationDate":"2015-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1109/BIBM.2015.7359913","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34313626","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: 10
Insight: Semantic Provenance and Analysis Platform for Multi-center Neurology Healthcare Research. Insight:多中心神经保健研究的语义来源和分析平台。
Proceedings. IEEE International Conference on Bioinformatics and Biomedicine Pub Date : 2015-11-01 DOI: 10.1109/BIBM.2015.7359776
Priya Ramesh, Annan Wei, Elisabeth Welter, Yvan Bamps, Shelley Stoll, Ashley Bukach, Martha Sajatovic, Satya S Sahoo
{"title":"<i>Insight</i>: Semantic Provenance and Analysis Platform for Multi-center Neurology Healthcare Research.","authors":"Priya Ramesh,&nbsp;Annan Wei,&nbsp;Elisabeth Welter,&nbsp;Yvan Bamps,&nbsp;Shelley Stoll,&nbsp;Ashley Bukach,&nbsp;Martha Sajatovic,&nbsp;Satya S Sahoo","doi":"10.1109/BIBM.2015.7359776","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359776","url":null,"abstract":"<p><p><i>Insight</i> is a Semantic Web technology-based platform to support large-scale secondary analysis of healthcare data for neurology clinical research. <i>Insight</i> features the novel use of: (1) provenance metadata, which describes the history or origin of patient data, in clinical research analysis, and (2) support for patient cohort queries across multiple institutions conducting research in epilepsy, which is the one of the most common neurological disorders affecting 50 million persons worldwide. <i>Insight</i> is being developed as a healthcare informatics infrastructure to support a national network of eight epilepsy research centers across the U.S. funded by the U.S. Centers for Disease Control and Prevention (CDC). This paper describes the use of the World Wide Web Consortium (W3C) PROV recommendation for provenance metadata that allows researchers to create patient cohorts based on the provenance of the research studies. In addition, the paper describes the use of descriptive logic-based OWL2 epilepsy ontology for cohort queries with \"expansion of query expression\" using ontology reasoning. Finally, the evaluation results for the data integration and query performance are described using data from three research studies with 180 epilepsy patients. The experiment results demonstrate that <i>Insight</i> is a scalable approach to use Semantic provenance metadata for context-based data analysis in healthcare informatics.</p>","PeriodicalId":74563,"journal":{"name":"Proceedings. IEEE International Conference on Bioinformatics and Biomedicine","volume":"2015 ","pages":"731-736"},"PeriodicalIF":0.0,"publicationDate":"2015-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1109/BIBM.2015.7359776","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34393837","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: 6
A Hybrid Algorithm for Non-negative Matrix Factorization Based on Symmetric Information Divergence. 基于对称信息散度的非负矩阵分解混合算法。
Proceedings. IEEE International Conference on Bioinformatics and Biomedicine Pub Date : 2015-11-01 Epub Date: 2015-12-17 DOI: 10.1109/BIBM.2015.7359924
Karthik Devarajan, Nader Ebrahimi, Ehsan Soofi
{"title":"A Hybrid Algorithm for Non-negative Matrix Factorization Based on Symmetric Information Divergence.","authors":"Karthik Devarajan,&nbsp;Nader Ebrahimi,&nbsp;Ehsan Soofi","doi":"10.1109/BIBM.2015.7359924","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359924","url":null,"abstract":"<p><p>The objective of this paper is to provide a hybrid algorithm for non-negative matrix factorization based on a symmetric version of Kullback-Leibler divergence, known as <i>intrinsic information</i>. The convergence of the proposed algorithm is shown for several members of the exponential family such as the Gaussian, Poisson, gamma and inverse Gaussian models. The speed of this algorithm is examined and its usefulness is illustrated through some applied problems.</p>","PeriodicalId":74563,"journal":{"name":"Proceedings. IEEE International Conference on Bioinformatics and Biomedicine","volume":"2015 ","pages":"1658-1664"},"PeriodicalIF":0.0,"publicationDate":"2015-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1109/BIBM.2015.7359924","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35371696","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: 4
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