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arXiv 2021年

作者： Landa, Boris Zhang, Thomas T.C.K. Kluger, Yuval Program in Applied Mathematics Yale University United States Department of Electrical and Systems Engineering University of Pennsylvania United States Interdepartmental Program in Computational Biology and Bioinformatics Yale University United States Department of Pathology Yale University School of Medicine United States

Estimating the rank of a corrupted data matrix is an important task in data analysis, most notably for choosing the number of components in PCA. Significant progress on this task was achieved using random matrix theory by characterizing the spectral properties of large noise matrices. However, utilizing such tools is not straightforward when the data matrix consists of count random variables, e.g., Poisson, in which case the noise can be heteroskedastic with an unknown variance in each entry. In this work, we consider a Poisson random matrix with independent entries, and propose a simple procedure termed biwhitening for estimating the rank of the underlying signal matrix (i.e., the Poisson parameter matrix) without any prior knowledge. Our approach is based on the key observation that one can scale the rows and columns of the data matrix simultaneously so that the spectrum of the corresponding noise agrees with the standard Marchenko-Pastur (MP) law, justifying the use of the MP upper edge as a threshold for rank selection. Importantly, the required scaling factors can be estimated directly from the observations by solving a matrix scaling problem via the Sinkhorn-Knopp algorithm. Aside from the Poisson, our approach is extended to families of distributions that satisfy a quadratic relation between the mean and the variance, such as the generalized Poisson, binomial, negative binomial, gamma, and many others. This quadratic relation can also account for missing entries in the data. We conduct numerical experiments that corroborate our theoretical findings, and showcase the advantage of our approach for rank estimation in challenging regimes. Furthermore, we demonstrate the favorable performance of our approach on several real datasets of single-cell RNA sequencing (scRNA-seq), High-Throughput Chromosome Conformation Capture (Hi-C), and document topic *** Codes 62H12, 62H25. Copyright © 2021, The Authors. All rights reserved.

关键词： Random variables

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Investigating the Efficacy of Data Mining Techniques for Crowdsourced Biological Datasets

Investigating the Efficacy of Data Mining Techniques for Cro...

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IEEE MIT Undergraduate Research Technology Conference (URTC)

作者： Ilona Regan Dany Alkurdi Sarun Paisarnsrisomsuk Carolina Ruiz Elizabeth F. Ryder Rob Gegear Bioinformatics and Computational Biology Program Worcester Polytechnic Institute Worcester MA USA Princeton University Princeton NJ USA Worcester Polytechnic Institute Worcester MA USA University of Massachusetts Dartmouth Dartmouth MA USA

ISBN: (纸本)9781728158198

The rapid worldwide decline of wild pollinators over recent years poses a significant environmental threat due to the critical keystone role that pollinators play in terrestrial ecosystems. In order to gain insight into the major anthropogenic factors causing these declines, researchers have collected large amounts of ecological data. Yet, they often lack the computational tools needed to analyze the information contained in such datasets. We investigate various data analysis techniques for the Beecology Project, which is a citizen science based effort to rapidly collect data on foraging habits of bumblebee species native to Massachusetts. Different data mining approaches were explored, including association analysis, trend analysis, classification, regression, and clustering. It was found that different techniques were more suitable depending on the biological research question. Future work will focus on making tools utilizing these approaches available online through the Beecology website, where they can be used by the public to determine how best to protect our native pollinators and the diverse ecosystems they support.

关键词： Data analysis Conferences Ecosystems Market research Encoding Data mining Biological information theory

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Analysis of cancer omics data in a semantic web framework

Analysis of cancer omics data in a semantic web framework

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Workshop on Semantic Web Applications and Tools for Life Sciences 2010, SWAT4LS 2010

作者： Holford, Matthew E. McCusker, James P. Cheung, Kei-Hoi Krauthammer, Michael Interdepartmental Program in Computational Biology and Bioinformatics Yale University New Haven CT United States Department of Pathology Yale University New Haven CT United States Department of Computer Science Yale University New Haven CT United States Center for Medical Informatics Yale University New Haven CT United States Department of Genetics Yale University New Haven CT United States

Our work concerns the elucidation of the cancer (epi)genome, transcriptome and proteome to better understand the complex interplay between a cancer cell's molecular state and its response to anti-cancer therapy. To study the problem, we have previously focused on data warehousing technologies and statistical data integration. In this paper, we present recent work on extending our analytical capabilities using Semantic Web technology. A key new component presented here is a SPARQL endpoint to our existing data warehouse. This endpoint allows the merging of observed quantitative data with existing data from semantic knowledge sources such as Gene Ontology (GO). We show how such variegated quantitative and functional data can be integrated and accessed in a universal manner using Semantic Web tools. We also demonstrate how Description Logic (DL) reasoning can be used to infer previously unstated conclusions from existing knowledge bases. As proof of concept, we illustrate the ability of our setup to answer complex queries on resistance of cancer cells to Decitabine, a demethylating agent.

关键词： Semantic Web

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Formalizing the representation of immune exposures for human immunology studies 9

Formalizing the representation of immune exposures for human...

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9th International Conference on Biological Ontology, ICBO 2018

作者： Vita, Randi Overton, James A. Cheung, Kei-Hoi Kleinstein, Steven H. Peters, Bjoern Division for Vaccine Discovery San Diego Institute for Allergy and Immunology San DiegoCA United States Department of Emergency Medicine Yale Center for Medical Informatics Yale School of Medicine New HavenCT United States Department of Pathology Yale School of Medicine New HavenCT United States Interdepartmental Program in Computational Biology and Bioinformatics Yale University New HavenCT United States

Human immunology studies typically examine how immune exposures associated with vaccinations, infectious, allergic or autoimmune diseases, or transplantations perturb the immune system with the goal to develop diagnostic tools and therapeutic interventions. While there are established approaches to formally represent the experimental data generated in such studies, which often comprises gene expression data, flow cytometry data, or serology data, the description of the immune exposures themselves is not well standardized. We here present a formal approach to represent immune exposures at a high level of granularity. We capture the exposure process (e.g. 'vaccination' or 'occurrence of allergic disease'), exposure material (e.g. 'Tdap vaccine' or 'House dust mite'), and the associated disease name and stage (e.g. 'allergic rhinitis' and 'chronic'). This representation scheme has been used successfully in the IEDB and an extended version has been adopted by HIPC to capture studies in ImmPort. We are reporting here on this scheme, our ongoing attempts to map the terms used to existing ontologies, and the challenges encountered. © 2018 CEUR-WS.

关键词： Ontology

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A Path Analysis Model for Explaining Factors That Influence the Use of Masker among Commuting Workers Using KRL Commuter Line Bogor Jakarta

Research Square

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Research Square 2021年

作者： Kusmawan, David Andari, Shofi Indri Hapsari, S. Faculty Medicine and Health Science Universitas Jambi Indonesia Bioinformatics and Computational Biology Graduate Program Iowa State University United States Occupational Health and Safety Department Faculty of Public Health Universitas Indonesia Indonesia

Jakarta is one of the most air polluted cities in the world, it can increase the risk of healthy of commuting worker. As one of the most air polluted cities in the world, Jakarta is at high risk of its commuting worker’s health. They are at risk of being exposed to pollutant. This study aims to determine the factors influencing directly and indirectly to healthy behavior (using masker) for commuting workers who use the KRL Commuterline Bogor - Jakarta. A total of 155 respondents participated in the study and the collected data were then analyzed using descriptive and path analysis. Commuters are aware of the hazard potential related to air pollution during commuting were 137 people (88.4%). Commuters with good perception of pollution were 104 people (67.1%). Commuters used masker during commuting was 125 people (80.6%). Healthy behavior (using masker) in commuting worker using KRL Commuter Line were affected by some factors both directly and indirectly. Knowledge and commuting experience toward healthy behavior using masker were two variables with a significant direct influence on healthy behavior using masker, and knowledge was also the only mediated variable with a significant indirect effect of education to healthy behavior (using masker). © 2021, CC BY.

关键词： Pollution

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Classification of Multiple Time-Series via Boosting

Classification of Multiple Time-Series via Boosting

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IEEE Digital Signal Processing Workshop

作者： Patrick L. Harrington Arvind Rao Alfred O., Hero Bioinformatics Graduate Program University of Michigan Ann Arbor MI USA Lane Center of Computational Biology Carnegie Mellon University Pittsburgh PA USA Department of Statistics University of Michigan Ann Arbor MI USA

Much of modern machine learning and statistics research consists of extracting information from high-dimensional patterns. Often times, the large number of features that comprise this high-dimensional pattern are themselves vector valued, corresponding to sampled values in a time-series. Here, we present a classification methodology to accommodate multiple time-series using boosting. This method constructs an additive model by adaptively selecting basis functions consisting of a discriminating feature's full time-series. We present the necessary modifications to fisher linear discriminant analysis and least-squares, as base learners, to accommodate the weighted data in the proposed boosting procedure. We conclude by presenting the performance of our proposed method against a synthetic stochastic differential equation data set and a real world data set involving prediction of cancer patient susceptibility for a particular chemoradiotherapy.

关键词： Boosting Statistics Vectors Linear discriminant analysis Gene expression bioinformatics computational biology Machine learning Data mining Stochastic processes

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Perspectives on Human Population Structure at the Cusp of the Sequencing Era

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Genomics and Human Genetics 1000年第1期12卷 245-274页

作者： John Novembre Sohini Ramachandran *Both authors contributed equally. 1Department of Ecology and Evolutionary Biology and Interdepartmental Program on Bioinformatics University of California Los Angeles California 90403 email: jnovembre@ucla.edu 2Department of Ecology and Evolutionary Biology and Center for Computational Molecular Biology Brown University Providence Rhode Island 02912 email: sramachandran@brown.edu

Human groups show structured levels of genetic similarity as a consequence of factors such as geographical subdivision and genetic drift. Surveying this structure gives us a scientific perspective on human origins, sheds light on evolutionary processes that shape both human adaptation and disease, and is integral to effectively carrying out the mission of global medical genetics and personalized medicine. Surveys of population structure have been ongoing for decades, but in the past three years, single-nucleotide-polymorphism (SNP) array technology has provided unprecedented detail on human population structure at global and regional scales. These studies have confirmed well-known relationships between distantly related populations and uncovered previously unresolvable relationships among closely related human groups. SNPs represent the first dense genome-wide markers, and as such, their analysis has raised many challenges and insights relevant to the study of population genetics with whole-genome sequences. Here we draw on the lessons from these studies to anticipate the directions that will be most fruitful to pursue during the emerging whole-genome sequencing era.

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Decision fusion of circulating markers for breast cancer detection in premenopausal women

Decision fusion of circulating markers for breast cancer det...

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7th IEEE International Conference on bioinformatics and Bioengineering, BIBE

作者： Jesneck, Jonathan L. Mukherjee, Sayan Nolte, Loren W. Lokshin, Anna E. Marks, Jeffrey R. Lo, Joseph Department of Biomedical Engineering Department of Statistical Science Computational Biology and Bioinformatics Program Duke Advanced Imaging Labs. Institute for Genome Sciences and Policy Department of Computer Science Duke University Department of Electrical and Computer Engineering Division of Hematology/Oncology University of Pittsburgh School of Medicine University of Pittsburgh Cancer Institute Pittsburgh PA 15213 United States Department of Experimental Surgery Duke University Medical Center Medical Physics Graduate Program Duke University Durham NC 27708 United States

ISBN: (纸本)1424415098

Current mammographic screeningfor breast cancer is less effective for younger women. To complement mammography for premenopausal women, we investigated the feasibility screening test using 98 blood serum proteins. Because the data set was very noisy and contained only weak features, we used a classifier designed for noisy data: decision fusion. Decision fusion outperformed both a support vector machine (SVM) and linear regression with forward stepwise feature selection on all three two-class classification tasks: normal tissue vs. cancer, normal tissue vs. benign lesions, and benign lesions vs. cancer. Decision fusion detected cancer moderately well (AUC=0.84 on normal vs. cancer), demonstrating promise as a screening tool. Decision fusion also detected benign lesions similarly well (AUC=0.83 on normal vs. benign lesions) and was the only classifier to achieve any success in separating benign from malignant lesions (AUC=0.64 on benign vs. cancer). The classification results suggest that the assayed proteins are more indicative of a secondary effect, such as immune response, rather than specific for breast cancer. In conclusion, the decision fusion classifier demonstrated some promise in detecting breast lesions and outperformed other classifiers, especially for the very noisy classification problem of distinguishing benign from malignant lesions. ©2007 IEEE.

关键词： Tissue

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Solvatochromic biosensor reveals conformational changes of single molecules in living cells

Solvatochromic biosensor reveals conformational changes of s...

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2022生物物理大会

作者： Bei Liu Nicholas K.Pinkin Frederico M.Pimenta Shiqiong Hu Saygin Gulec Timothy C.Elston Klaus M.Hahn National Biomedical Imaging Center Peking University School of Future Technology Department of Pharmacology University of North Carolina at Chapel Hill School of Medicine Curriculum in Bioinformatics and Computational Biology University of North Carolina at Chapel Hill Computational Medicine Program University of North Carolina at Chapel Hill

Revealing the activity or conformation while following the diffusion of individual proteins inside living cells is challenging, demanding biosensors that are sensitive,easy to deploy, and versatile. GTPases are switch... 详细信息

关键词： Solvatochromic biosensor reveals conformational changes of single molecules in living cells

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Deciphering sequence and structure features of disease-causing small insertions and deletions

Deciphering sequence and structure features of disease-causi...

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第五届全国生物信息学与系统生物学学术大会

作者： Xinjun Zhang Huiying Zhao Yadong Wang Guohua Wang Yaoqi Zhou Yunlong Liu School of Computer Sciences and Technology Harbin Institute of Technology Harbin Heilongjiang 150001 China School of Informatics and Computing Indiana University Bloomington IN 47408 USA School of Computer Sciences and Technology Harbin Institute of Technology Harbin Heilongjiang 150001 China Center for Computational Biology and Bioinformatics Indiana University School of Medicine Indianapolis IN 46202 USA Bioinformatics program School of Informatics Indiana University Purdue University Indianapolis Indianapolis IN 46202 USA Department of Medical and Molecular Genetics Indiana University School of Medicine Indianapolis IN 46202 USA Center for Computational Biology and Bioinformatics Indiana University School of Medicine Indianapolis IN 46202 USA Center for Computational Biology and Bioinformatics Indiana University School of Medicine Indianapolis IN 46202 USA

Background: Small insertions and deletions (INDELs) compose of the second largest category of genetic variants (next to single nucleotide polymorphism) in the human genome, which accounts for 18% of all the variants *** from the 1,000 Genome Project indicated an estimate of 1 million INDELs per human *** to SNPs (Single Nucleotide Polymorphisms) and large structural variations, INDELs are of significant interest due to their potentials in affecting gene molecular functions and therefore cause *** of its functional importance, lacking a highly accurate bioinformatics tool for INDEL classifications has become a major obstacle in understanding the molecular ***: In this study, we develop a bioinformatics tool for INDEL *** constructed a training dataset that includes all the disease-causing and neutral INDELs documented in the Human Genome Mutation Database (HGMD) and 1,000 Genome *** the two sets of INDELs, we systematically investigated a series of features on their potentials in disrupting both protein structures and pre-mRNA *** then designed a predictor to best distinguish the disease-causing and neutral INDELs using machine-learning ***: In this study, we focused on the disease relevance of the INDELs in the exonic regions, which include 25,923 and 4,643 disease-causing and neutral INDELs, *** found that the disease-causing INDELs more likely occur in predicted structured regions and neutral INDELs are more likely in unstructured, intrinsically disordered *** also found that INDEL sites matched more to homologous sequences are more like *** RNA processing, we found disease-causing INDELs are twice likely to disrupt binding sites of RNA-binding *** also found that disease-causing INDELs tend to be longer, and be closer to the splice *** addition, the genomic loci for disease-causing INDELs are more evolutionarily conserved, a

关键词： insertion deletions INDELs genetic variants next generation sequencing

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