2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)最新文献

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A domain ontology for the Non-Coding RNA field 非编码RNA领域的领域本体
2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Pub Date : 2015-11-09 DOI: 10.1109/BIBM.2015.7359755
Jingshan Huang, K. Eilbeck, J. Blake, D. Dou, D. Natale, A. Ruttenberg, Barry Smith, Michael T. Zimmermann, Guoqian Jiang, Yu Lin, Bin Wu, Y. He, Shaojie Zhang, Xiaowei Wang, He Zhang, Zixing Liu, M. Tan
{"title":"A domain ontology for the Non-Coding RNA field","authors":"Jingshan Huang, K. Eilbeck, J. Blake, D. Dou, D. Natale, A. Ruttenberg, Barry Smith, Michael T. Zimmermann, Guoqian Jiang, Yu Lin, Bin Wu, Y. He, Shaojie Zhang, Xiaowei Wang, He Zhang, Zixing Liu, M. Tan","doi":"10.1109/BIBM.2015.7359755","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359755","url":null,"abstract":"Identification of non-coding RNAs (ncRNAs) has been significantly enhanced due to the rapid advancement in sequencing technologies. On the other hand, semantic annotation of ncRNA data lag behind their identification, and there is a great need to effectively integrate discovery from relevant communities. To this end, the Non-Coding RNA Ontology (NCRO) is being developed to provide a precisely defined ncRNA controlled vocabulary, which can fill a specific and highly needed niche in unification of ncRNA biology.","PeriodicalId":186217,"journal":{"name":"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","volume":"37 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123881228","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: 2
A seeding-searching-ensemble method for gland segmentation and detection 一种用于腺体分割和检测的种子搜索集成方法
2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Pub Date : 2015-11-09 DOI: 10.1109/BIBM.2015.7359707
Yizhe Zhang, L. Yang, J. MacKenzie, R. Ramachandran, D. Chen
{"title":"A seeding-searching-ensemble method for gland segmentation and detection","authors":"Yizhe Zhang, L. Yang, J. MacKenzie, R. Ramachandran, D. Chen","doi":"10.1109/BIBM.2015.7359707","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359707","url":null,"abstract":"Glands are vital tissues found throughout the human body and their structure and function are affected by many diseases. The ability to segment and detect glands among other types of tissues is important for the study of normal and disease processes and is readily visualized by pathologists in microscopic detail. In this paper, we develop a new approach for segmenting and detecting intestinal glands in H&E stained histology images, which utilizes a set of advanced image processing techniques such as graph search, ensemble, feature extraction and classification. Our method computes fast, and is able to preserve gland boundaries robustly and detect glands accurately. We tested the performance of gland detection and segmentation by analyzing a dataset of 1723 glands from digitized high-resolution clinical histology images obtained in normal and diseased intestines. The experimental results show that our method outperforms considerably the state-of-the-art methods for gland segmentation and detection tasks.","PeriodicalId":186217,"journal":{"name":"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","volume":"63 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125335532","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: 0
A path based approach to quantifying the progression of Alzheimer's disease 基于路径的方法量化阿尔茨海默病的进展
2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Pub Date : 2015-11-09 DOI: 10.1109/BIBM.2015.7359826
Prabesh Kanel, Xiuwen Liu
{"title":"A path based approach to quantifying the progression of Alzheimer's disease","authors":"Prabesh Kanel, Xiuwen Liu","doi":"10.1109/BIBM.2015.7359826","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359826","url":null,"abstract":"Histological studies suggest that different pathological changes occur in the subfields of hippocampi in aging and in Alzheimer0s disease. The pathological changes due to Alzheimer's disease follows a neural system and are consistent with subjects. The aim of this study is to study the path in vivo the changes in normal control, mild cognitive impairment and Alzheimers disease patients using high resolution MRI scanned at 3 Tesla. T1 weighted images were obtained from the ADNI database. The dataset consists of 11 control patients, 13 MCI patients, and 9 AD patients. The hippocampal subfields were segmented using the Freesurfer image-analysis suite (Version 6.0). The volume of the subfields and the path along the medial axis of the subfields were studied. The results suggest that the intensity along the medial axis shows more variation on the CA1 region than other subfields in cases of Alzheimer disease, MCI and normal control patients. The changes are more prominent in the early section of the CA1 suggesting the progressive nature of the disease. The mean intensity value along the medial axis of CA1 subfield shows change in AD, MCI and NC but similar change are not seen in other subfields.","PeriodicalId":186217,"journal":{"name":"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","volume":"67 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125560697","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: 0
The syndromes of lung cancer and compatibility of medicine in Traditional Chinese Medicine science treatment based on Clustering Algorithm 基于聚类算法的中医治疗肺癌证候与药物配伍
2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Pub Date : 2015-11-09 DOI: 10.1109/BIBM.2015.7359830
Miao Wang, Mengying Wang, Dongyi Wang, S. Duan, Yisheng Wang, Yanjun Huang, Huiliang Shang
{"title":"The syndromes of lung cancer and compatibility of medicine in Traditional Chinese Medicine science treatment based on Clustering Algorithm","authors":"Miao Wang, Mengying Wang, Dongyi Wang, S. Duan, Yisheng Wang, Yanjun Huang, Huiliang Shang","doi":"10.1109/BIBM.2015.7359830","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359830","url":null,"abstract":"As the study for the modernization of Traditional Chinese Medicine (TCM) is moving continuously forward, a growing bond exists between TCM and modern information processing technology. The determination of syndrome and the study for the compatibility of medicines in TCM are main parts of it. In this paper, we clustered syndromes of lung cancer patients according to the clinical based cases by adopting Clustering Algorithm Based On Sparse Feature Vector algorithm (CABOSFV) algorithm and concluded three TCM classifications for lung cancer. Moreover, by the further study of the compatibility of medicines, numerous matches for critical medicines were proposed, and the results are correspond to clinical data.","PeriodicalId":186217,"journal":{"name":"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126168449","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: 2
Structuring unstructured clinical narratives in OpenMRS with medical concept extraction 利用医学概念提取在OpenMRS中构建非结构化临床叙述
2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Pub Date : 2015-11-09 DOI: 10.1109/BIBM.2015.7359782
R. Eshleman, Hui Yang, Barry Levine
{"title":"Structuring unstructured clinical narratives in OpenMRS with medical concept extraction","authors":"R. Eshleman, Hui Yang, Barry Levine","doi":"10.1109/BIBM.2015.7359782","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359782","url":null,"abstract":"We have developed a new software module for the open source Electronic Medical Record System OpenMRS to analyze unstructured clinical narratives. This module leverages Named Entity Recognition (NER) to deliver concise, semantic-type driven, interactive summaries of clinical notes. To this end, we performed an extensive empirical evaluation of four Named Entity Recognition (NER) systems using textual clinical narratives and full biomedical journal articles. The four NER systems under evaluation are MetaMap, cTAKES, BANNER. We studied several ensemble approaches built upon the above four NER systems to exploit their collaborative strengths. Evaluations are performed on the manually annotated patient discharge summaries from the Informatics for Integrating Biology and the Bedside group (I2B2) and the CRAFT dataset. The main results include (1) BANNER significantly outperforms the other three systems on the I2B2 dataset with F1 values in the range of .73-.89, in contrast to .28 - .60 of other systems; and (2) Surprisingly, an ensemble approach of BANNER with any combinations of the other three approaches tends to degrade the performance by .08 - .11 in F1 when evaluated on the I2B2 dataset. Based on the evaluation results, we have developed a BANNER-based NER module for OpenMRS to recognize semantic concepts including problems, tests, and treatments. This module works with OpenMRS versions 2.×. The user interface presents concise clinical notes summaries and allows the user to filter, search and view the context of the concepts. We have also developed a companion web application to retrain the BANNER model using data from OpenMRS. The module and source code are available at wiki.openmrs.org/display/docs/Visit+Notes+Analysis+Module.","PeriodicalId":186217,"journal":{"name":"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125834664","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: 4
ENISI multiscale modeling of mucosal immune responses driven by high performance computing 高性能计算驱动的ENISI粘膜免疫反应多尺度建模
2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Pub Date : 2015-11-09 DOI: 10.1109/BIBM.2015.7359768
V. Abedi, R. Hontecillas, S. Hoops, Nathan Liles, Adria Carbo, Pinyi Lu, C. Philipson, J. Bassaganya-Riera
{"title":"ENISI multiscale modeling of mucosal immune responses driven by high performance computing","authors":"V. Abedi, R. Hontecillas, S. Hoops, Nathan Liles, Adria Carbo, Pinyi Lu, C. Philipson, J. Bassaganya-Riera","doi":"10.1109/BIBM.2015.7359768","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359768","url":null,"abstract":"Computational modeling tools have increasingly important roles in our understanding of biological processes. Computer simulations guide experimental and clinical efforts in an unprecedented rate. This study presents ENteric Immunity Simulator - multiscale modeling (MSM) platform developed for high performance computing (HPC). ENISI MSMv2 is designed for modeling mucosal immune responses. The system scales to 109 agents in HPC simulations. This is an important step towards building large scale information processing representations of immune responses that integrate multiple modeling technologies and spatiotemporal scales ranging from nanoseconds to years and from molecules to systems. Our HPC-driven ENISI MSM platform combines the study of molecular pathways controlling T cell differentiation and tissue level interactions between cells to characterize novel mechanisms of immunoregulation at the gut mucosa.","PeriodicalId":186217,"journal":{"name":"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","volume":"30 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130890463","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
Comparative study of Middle East respiratory syndrome coronavirus using bioinformatics techniques 利用生物信息学技术对中东呼吸综合征冠状病毒的比较研究
2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Pub Date : 2015-11-09 DOI: 10.1109/BIBM.2015.7359937
Insung Ahn, Jinhwa Jang
{"title":"Comparative study of Middle East respiratory syndrome coronavirus using bioinformatics techniques","authors":"Insung Ahn, Jinhwa Jang","doi":"10.1109/BIBM.2015.7359937","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359937","url":null,"abstract":"In this study, we collected 141 coding sequences of MERS-CoV from the National Center for Biotechnology and Information (NCBI), including the sequences isolated in Korea in 2015. We conducted the phylogenetic analysis using the Maximum Likelihood method to examine the overall variation patterns among the target sequences, and then, we divided the target sequences into 4 different groups according to occurred countries and host species. Using the codon analyzer named SimFluVar program, we analyzed the codon variation patterns in the wobble position among 4 groups. In order to investigate the effect of codon variations that can change the phenotype of target genes, we compared the transversional substitutions between the Korean-origin sequences and other groups. As a result, we found that the Korea-origin sequences showed very minor differences with those collected from the Saudi Arabia in 2015, whereas other groups which were collected from USA and UK in 2013 and 2014 showed more complicated differences. We also compared the Korea-origin sequences with those of camel-origin sequences, and we found that the substitution pattern was somewhat different with that of human-origin viruses.","PeriodicalId":186217,"journal":{"name":"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130166346","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: 4
Parallel group ICA for multimodal biomedical data analyses 用于多模态生物医学数据分析的平行组ICA
2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Pub Date : 2015-11-09 DOI: 10.1109/BIBM.2015.7359832
Jingyu Liu, Jiayu Chen, V. Calhoun
{"title":"Parallel group ICA for multimodal biomedical data analyses","authors":"Jingyu Liu, Jiayu Chen, V. Calhoun","doi":"10.1109/BIBM.2015.7359832","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359832","url":null,"abstract":"Multiple types of signals or images are often collected from the same participants in biomedical research. Multimodal analyses have been shown to better capture the joint information. We propose a new method named parallel group independent component analysis (para-GICA) to address a special need for parallel processing of multimodal brain images or signals where it is desirable to partition into groups, for example to stratify by age. Para-GICA is designed to identify associated components between two modalities based on their loading variations in participants, while allowing components to show group specificity. Simulation using synthetic MRI and genetic data demonstrates that para-GICA is able to recover group specific brain networks and the connection between brain networks and genetic factors. A real data application on brain gray matter concentration and whiter matter fractional anisotropy images extracts associated gray matter and white matter components, and ageing induced spatial differences of the components.","PeriodicalId":186217,"journal":{"name":"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","volume":"55 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128687171","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: 0
Feature selection of high-dimensional biomedical data using improved SFLA for disease diagnosis 基于改进SFLA的高维生物医学数据特征选择用于疾病诊断
2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Pub Date : 2015-11-09 DOI: 10.1109/BIBM.2015.7359728
Yongqiang Dai, Bin Hu, Yun Su, Chengsheng Mao, Jing Chen, Xiaowei Zhang, P. Moore, Lixin Xu, Hanshu Cai
{"title":"Feature selection of high-dimensional biomedical data using improved SFLA for disease diagnosis","authors":"Yongqiang Dai, Bin Hu, Yun Su, Chengsheng Mao, Jing Chen, Xiaowei Zhang, P. Moore, Lixin Xu, Hanshu Cai","doi":"10.1109/BIBM.2015.7359728","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359728","url":null,"abstract":"High-dimensional biomedical datasets contain thousands of features used in molecular disease diagnosis, however many irrelevant or weak correlation features influence the predictive accuracy. Feature selection algorithms enable classification techniques to accurately identify patterns in the features and find a feature subset from an original set of features without reducing the predictive classification accuracy while reducing the computational overhead in data mining. In this paper we present an improved shuffled frog leaping algorithm (ISFLA) which explores the space of possible subsets to obtain the set of features that maximizes the predictive accuracy and minimizes irrelevant features in high-dimensional biomedical data. Evaluation employs the K-nearest neighbour approach and a comparative analysis with a genetic algorithm, particle swarm optimization and the shuffled frog leaping algorithm shows that our improved algorithm achieves improvements in the identification of relevant subsets and in classification accuracy.","PeriodicalId":186217,"journal":{"name":"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","volume":"33 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121851369","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: 16
SRP: A concise non-parametric similarity-rank-based model for predicting drug-target interactions SRP:用于预测药物-靶标相互作用的简洁非参数相似性排序模型
2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Pub Date : 2015-11-09 DOI: 10.1109/BIBM.2015.7359921
Jianyu Shi, S. Yiu
{"title":"SRP: A concise non-parametric similarity-rank-based model for predicting drug-target interactions","authors":"Jianyu Shi, S. Yiu","doi":"10.1109/BIBM.2015.7359921","DOIUrl":"https://doi.org/10.1109/BIBM.2015.7359921","url":null,"abstract":"The identification of drug-target interactions in web lab is costly and time-consuming. Computational approaches become important to help identifying potential candidates for laboratory experiments. However, they usually involve solving optimization problems or assuming statistical distribution based on prior knowledge, and may require estimating tunable parameters. This paper is motivated by the concepts behind “follow-on” drugs. They are the drugs developed by drug companies to substitute the pioneering drug which was firstly discovered and patented for a specific target and determined a new therapeutic class. There are three observations from “follow-on” drugs. The first observation has been used by many existing methods: drugs interacting with a common target usually have higher similar scores (e.g. the similarity score in terms of chemical structure). The second one is that a drug candidate for a specific target gains more attention if it is more similar to those drugs interacting with the target than other known drugs, even though the similarity score is low. Lastly, people intuitively tend to design a “follow-on” drug for the targets already having more drugs because of less cost and less risk. In our approach, the above observations are translated into more evidences for predicted drug-target interaction. Designing an interaction tendency index to characterize these observations, we propose the similarity-rank-based predictor (SRP). Unlike other models, SRP is a non-parametric model and requires neither solving an optimization problem nor prior statistical knowledge. Based on real benchmark datasets, we show that our model is able to achieve higher accuracy than the two most recent models and our approach is able to cope with two real predicting scenario of missing interactions.","PeriodicalId":186217,"journal":{"name":"2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","volume":"17 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121137291","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: 14
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