Download or read book Machine learning based methods for RNA data analysis volume II written by Lihong Peng and published by Frontiers Media SA. This book was released on 2023-01-02 with total page 164 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Machine learning based methods for RNA data analysis volume III written by Lihong Peng and published by Frontiers Media SA. This book was released on 2023-02-17 with total page 134 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Machine Learning Based Methods for RNA Data Analysis written by Lihong Peng and published by Frontiers Media SA. This book was released on 2022-06-16 with total page 124 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Gene Expression Data Analysis written by Pankaj Barah and published by CRC Press. This book was released on 2021-11-08 with total page 276 pages. Available in PDF, EPUB and Kindle. Book excerpt: Development of high-throughput technologies in molecular biology during the last two decades has contributed to the production of tremendous amounts of data. Microarray and RNA sequencing are two such widely used high-throughput technologies for simultaneously monitoring the expression patterns of thousands of genes. Data produced from such experiments are voluminous (both in dimensionality and numbers of instances) and evolving in nature. Analysis of huge amounts of data toward the identification of interesting patterns that are relevant for a given biological question requires high-performance computational infrastructure as well as efficient machine learning algorithms. Cross-communication of ideas between biologists and computer scientists remains a big challenge. Gene Expression Data Analysis: A Statistical and Machine Learning Perspective has been written with a multidisciplinary audience in mind. The book discusses gene expression data analysis from molecular biology, machine learning, and statistical perspectives. Readers will be able to acquire both theoretical and practical knowledge of methods for identifying novel patterns of high biological significance. To measure the effectiveness of such algorithms, we discuss statistical and biological performance metrics that can be used in real life or in a simulated environment. This book discusses a large number of benchmark algorithms, tools, systems, and repositories that are commonly used in analyzing gene expression data and validating results. This book will benefit students, researchers, and practitioners in biology, medicine, and computer science by enabling them to acquire in-depth knowledge in statistical and machine-learning-based methods for analyzing gene expression data. Key Features: An introduction to the Central Dogma of molecular biology and information flow in biological systems A systematic overview of the methods for generating gene expression data Background knowledge on statistical modeling and machine learning techniques Detailed methodology of analyzing gene expression data with an example case study Clustering methods for finding co-expression patterns from microarray, bulkRNA, and scRNA data A large number of practical tools, systems, and repositories that are useful for computational biologists to create, analyze, and validate biologically relevant gene expression patterns Suitable for multidisciplinary researchers and practitioners in computer science and the biological sciences

Download or read book Classification in BioApps written by Nilanjan Dey and published by Springer. This book was released on 2017-11-10 with total page 453 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book on classification in biomedical image applications presents original and valuable research work on advances in this field, which covers the taxonomy of both supervised and unsupervised models, standards, algorithms, applications and challenges. Further, the book highlights recent scientific research on artificial neural networks in biomedical applications, addressing the fundamentals of artificial neural networks, support vector machines and other advanced classifiers, as well as their design and optimization. In addition to exploring recent endeavours in the multidisciplinary domain of sensors, the book introduces readers to basic definitions and features, signal filters and processing, biomedical sensors and automation of biomeasurement systems. The target audience includes researchers and students at engineering and medical schools, researchers and engineers in the biomedical industry, medical doctors and healthcare professionals.

Download or read book Computational methods for microbiome analysis volume 2 written by Setubal and published by Frontiers Media SA. This book was released on 2023-01-04 with total page 223 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Machine Learning Techniques on Gene Function Prediction Volume II written by Quan Zou and published by Frontiers Media SA. This book was released on 2023-04-11 with total page 264 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Machine Learning in Single Cell RNA seq Data Analysis written by Khalid Raza and published by Springer Nature. This book was released on with total page 104 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book System Biology Methods and Tools for Integrating Omics Data Volume II written by Liang Cheng and published by Frontiers Media SA. This book was released on 2022-09-07 with total page 158 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Handbook of Machine Learning Applications for Genomics written by Sanjiban Sekhar Roy and published by Springer Nature. This book was released on 2022-06-23 with total page 222 pages. Available in PDF, EPUB and Kindle. Book excerpt: Currently, machine learning is playing a pivotal role in the progress of genomics. The applications of machine learning are helping all to understand the emerging trends and the future scope of genomics. This book provides comprehensive coverage of machine learning applications such as DNN, CNN, and RNN, for predicting the sequence of DNA and RNA binding proteins, expression of the gene, and splicing control. In addition, the book addresses the effect of multiomics data analysis of cancers using tensor decomposition, machine learning techniques for protein engineering, CNN applications on genomics, challenges of long noncoding RNAs in human disease diagnosis, and how machine learning can be used as a tool to shape the future of medicine. More importantly, it gives a comparative analysis and validates the outcomes of machine learning methods on genomic data to the functional laboratory tests or by formal clinical assessment. The topics of this book will cater interest to academicians, practitioners working in the field of functional genomics, and machine learning. Also, this book shall guide comprehensively the graduate, postgraduates, and Ph.D. scholars working in these fields.

Download or read book Computational Methods for Next Generation Sequencing Data Analysis written by Ion Mandoiu and published by John Wiley & Sons. This book was released on 2016-09-12 with total page 464 pages. Available in PDF, EPUB and Kindle. Book excerpt: Introduces readers to core algorithmic techniques for next-generation sequencing (NGS) data analysis and discusses a wide range of computational techniques and applications This book provides an in-depth survey of some of the recent developments in NGS and discusses mathematical and computational challenges in various application areas of NGS technologies. The 18 chapters featured in this book have been authored by bioinformatics experts and represent the latest work in leading labs actively contributing to the fast-growing field of NGS. The book is divided into four parts: Part I focuses on computing and experimental infrastructure for NGS analysis, including chapters on cloud computing, modular pipelines for metabolic pathway reconstruction, pooling strategies for massive viral sequencing, and high-fidelity sequencing protocols. Part II concentrates on analysis of DNA sequencing data, covering the classic scaffolding problem, detection of genomic variants, including insertions and deletions, and analysis of DNA methylation sequencing data. Part III is devoted to analysis of RNA-seq data. This part discusses algorithms and compares software tools for transcriptome assembly along with methods for detection of alternative splicing and tools for transcriptome quantification and differential expression analysis. Part IV explores computational tools for NGS applications in microbiomics, including a discussion on error correction of NGS reads from viral populations, methods for viral quasispecies reconstruction, and a survey of state-of-the-art methods and future trends in microbiome analysis. Computational Methods for Next Generation Sequencing Data Analysis: Reviews computational techniques such as new combinatorial optimization methods, data structures, high performance computing, machine learning, and inference algorithms Discusses the mathematical and computational challenges in NGS technologies Covers NGS error correction, de novo genome transcriptome assembly, variant detection from NGS reads, and more This text is a reference for biomedical professionals interested in expanding their knowledge of computational techniques for NGS data analysis. The book is also useful for graduate and post-graduate students in bioinformatics.

Download or read book Benchmarking Statistical and Machine Learning Methods for Single cell RNA Sequencing Data written by Nan Xi and published by . This book was released on 2021 with total page 203 pages. Available in PDF, EPUB and Kindle. Book excerpt: The large-scale, high-dimensional, and sparse single-cell RNA sequencing (scRNA-seq) data have raised great challenges in the pipeline of data analysis. A large number of statistical and machine learning methods have been developed to analyze scRNA-seq data and answer related scientific questions. Although different methods claim advantages in certain circumstances, it is difficult for users to select appropriate methods for their analysis tasks. Benchmark studies aim to provide recommendations for method selection based on an objective, accurate, and comprehensive comparison among cutting-edge methods. They can also offer suggestions for further methodological development through massive evaluations conducted on real data. In Chapter 2, we conduct the first, systematic benchmark study of nine cutting-edge computational doublet-detection methods. In scRNA-seq, doublets form when two cells are encapsulated into one reaction volume by chance. The existence of doublets, which appear as but are not real cells, is a key confounder in scRNA-seq data analysis. Computational methods have been developed to detect doublets in scRNA-seq data; however, the scRNA-seq field lacks a comprehensive benchmarking of these methods, making it difficult for researchers to choose an appropriate method for their specific analysis needs. Our benchmark study compares doublet-detection methods in terms of their detection accuracy under various experimental settings, impacts on downstream analyses, and computational efficiency. Our results show that existing methods exhibited diverse performance and distinct advantages in different aspects. In Chapter 3, we develop an R package DoubletCollection to integrate the installation and execution of different doublet-detection methods. Traditional benchmark studies can be quickly out-of-date due to their static design and the rapid growth of available methods. DoubletCollection addresses this issue in benchmarking doublet-detection methods for scRNA-seq data. DoubletCollection provides a unified interface to perform and visualize downstream analysis after doublet-detection. Additionally, we created a protocol using DoubletCollection to execute and benchmark doublet-detection methods. This protocol can automatically accommodate new doublet-detection methods in the fast-growing scRNA-seq field. In Chapter 4, we conduct the first comprehensive empirical study to explore the best modeling strategy for autoencoder-based imputation methods specific to scRNA-seq data. The autoencoder-based imputation method is a family of promising methods to denoise sparse scRNA-seq data; however, the design of autoencoders has not been formally discussed in the literature. Current autoencoder-based imputation methods either borrow the practice from other fields or design the model on an ad hoc basis. We find that the method performance is sensitive to the key hyperparameter of autoencoders, including architecture, activation function, and regularization. Their optimal settings on scRNA-seq are largely different from those on other data types. Our results emphasize the importance of exploring hyperparameter space in such complex and flexible methods. Our work also points out the future direction of improving current methods.

Download or read book Intelligent Computing Theories and Application written by De-Shuang Huang and published by Springer Nature. This book was released on 2020-10-13 with total page 638 pages. Available in PDF, EPUB and Kindle. Book excerpt: This two-volume set of LNCS 12463 and LNCS 12464 constitutes - in conjunction with the volume LNAI 12465 - the refereed proceedings of the 16th International Conference on Intelligent Computing, ICIC 2020, held in Bari, Italy, in October 2020. The 162 full papers of the three proceedings volumes were carefully reviewed and selected from 457 submissions. The ICIC theme unifies the picture of contemporary intelligent computing techniques as an integral concept that highlights the trends in advanced computational intelligence and bridges theoretical research with applications. The theme for this conference is “Advanced Intelligent Computing Methodologies and Applications.” Papers related to this theme are especially solicited, addressing theories, methodologies, and applications in science and technology.

Download or read book MacHine Learning Based Sequence Analysis Bioinformatics and Nanopore Transduction Detection written by Stephen Winters-Hilt and published by Lulu.com. This book was released on 2011-05-01 with total page 436 pages. Available in PDF, EPUB and Kindle. Book excerpt: This is intended to be a simple and accessible book on machine learning methods and their application in computational genomics and nanopore transduction detection. This book has arisen from eight years of teaching one-semester courses on various machine-learning, cheminformatics, and bioinformatics topics. The book begins with a description of ad hoc signal acquisition methods and how to orient on signal processing problems with the standard tools from information theory and signal analysis. A general stochastic sequential analysis (SSA) signal processing architecture is then described that implements Hidden Markov Model (HMM) methods. Methods are then shown for classification and clustering using generalized Support Vector Machines, for use with the SSA Protocol, or independent of that approach. Optimization metaheuristics are used for tuning over algorithmic parameters throughout. Hardware implementations and short code examples of the various methods are also described.

Download or read book Machine Learning Methods for Single cell RNA sequencing Data Analysis written by Chuanqi Wang and published by . This book was released on 2021 with total page 103 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Advanced interpretable machine learning methods for clinical NGS big data of complex hereditary diseases volume II written by Yudong Cai and published by Frontiers Media SA. This book was released on 2023-02-13 with total page 194 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Machine Learning Techniques on Gene Function Prediction written by Quan Zou and published by Frontiers Media SA. This book was released on 2019-12-04 with total page 485 pages. Available in PDF, EPUB and Kindle. Book excerpt: