Integrative omics : concepts, methodology and application /

Provides a holistic and integrated view of defining and applying network approaches, integrative tools, and methods to solve problems for the rationalization of genotype to phenotype relationships. The reference provides systemic 'step-by-step' coverage that begins with basic concepts from...

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Bibliographic Details
Corporate Author: ScienceDirect (Online service)
Other Authors: Gupta, Manish Kumar (Editor), Katara, Pramod (Editor), Mondal, Sukanta (Editor), Singh, Ram Lakhan (Editor)
Format: eBook
Language:English
Published: London, United Kingdom : San Diego, CA : Academic Press, [2024]
Subjects:
Online Access:Connect to the full text of this electronic book
Table of Contents:
  • Front Cover
  • Integrative Omics
  • Integrative Omics: Concept, Methodology and Application
  • Copyright
  • Dedication
  • Contents
  • List of contributors
  • Preface
  • Organization of the book
  • 1
  • From omic to multi-integrative omics approach
  • 1. Introduction
  • 1.1 Omics
  • 1.2 Genomics
  • 1.3 Transcriptomics
  • 1.4 Proteomics
  • 1.5 Metabolomics
  • 1.6 Epigenomics
  • 1.7 Other potential omics
  • 1.7.1 Fluxomics
  • 1.7.2 Interactomics
  • 1.7.3 Metagenomics
  • 1.7.4 Pharmacogenomics
  • 1.7.5 Phenomics
  • 1.7.6 Foodomics
  • 2. From omics to multi-integrative omics
  • 3. Potential of multi-integrative omics
  • 4. Integration and interdependencies of omics
  • 4.1 Postanalysis data integration approaches
  • 4.2 Integrated data analysis approaches
  • 5. Data for multi-integrative omics
  • 5.1 Multiomics data
  • 5.2 Integration of multiomics data
  • 6. Data mining and exploitation for omics data
  • 7. Data mining tools/software
  • 8. Integrative data mining challenges and possibilities
  • 9. Scope for data science in multi-integrative omics
  • 10. Conclusion
  • References
  • 2
  • Types of omics data: Genomics, metagenomics, epigenomics, transcriptomics, proteomics, metabolomics, and phenom ...
  • 1. Introduction
  • 1.1 Genomics
  • 1.2 Transcriptomics
  • 1.3 Proteomics
  • 1.4 Metabolomics
  • 1.5 Epigenomics
  • 2. Genomics in medicine
  • 2.1 Current trends of genomics in medicine
  • 2.1.1 Precision medicine
  • 2.1.2 Pharmacogenomics
  • 2.1.3 Genome editing
  • 2.1.4 Gene therapy
  • 2.2 Computational pipeline for genomics using R code
  • 2.3 Applications of genomics
  • 3. Metagenomics
  • 3.1 Computational pipeline for metagenomics
  • 3.2 Metagenomics omics tools and packages
  • 4. Epigenomics
  • 4.1 Publicly available datasets for epigenomics studies
  • 4.1.1 The ENCODE project
  • 4.1.2 The Roadmap Epigenomics project
  • 4.1.3 The BLUEPRINT project.
  • 4.1.4 The NIH Epigenomics Data Analysis and Coordination Center
  • 4.1.5 The Gene Expression Omnibus
  • 4.2 Epigenomics omics approaches
  • 4.2.1 DNA methylation omics approaches
  • 4.2.2 R code for DNA methylation data analysis pipeline
  • 4.3 Epigenetic gene ontology and pathway analyses
  • 4.4 Epigenomics databases
  • 4.5 R codes for epigenomics data analysis
  • 5. Transcriptomics
  • 5.1 Transcriptomics studies in medicine
  • 5.2 Publicly available transcriptomics datasets
  • 5.2.1 GEO
  • 5.2.2 The Cancer Genome Atlas
  • 5.2.3 ArrayExpress
  • 5.3 Transcriptomics computational pipelines
  • 6. Proteomics
  • 6.1 Omics approaches for proteomics
  • 6.1.1 Quantitative proteomics
  • 6.1.2 Structural proteomics
  • 6.1.3 Posttranslational modification proteomics
  • 6.1.4 Functional proteomics
  • 7. Metabolomics
  • 7.1 Types of metabolomics
  • 7.1.1 Untargeted metabolomics
  • 7.1.2 Targeted metabolomics
  • 7.2 Various approaches commonly used in metabolomics
  • 7.3 R codes for metabolomics pipeline
  • 7.4 Publicly available metabolomics datasets
  • 7.5 Application of omics-based metabolomics tools
  • 8. Phenomics
  • 8.1 Phenomics example datasets for using in R
  • 8.2 Omics pipeline for phenomics analysis
  • References
  • 3
  • Biological omics databases and tools
  • 1. Introduction
  • 2. Omics datasets study based on different technology
  • 2.1 Next-generation sequencing
  • 2.2 Microarray
  • 2.3 RNA-Seq
  • 2.4 Mass spectrometry
  • 2.5 GC-MS (gas chromatography MS), LC-MS (liquid chromatography MS), and CE-MS (capillary electrophoresis MS)
  • 3. Specific omics datasets based on sequencing approach
  • 3.1 Genomics
  • 3.2 Epigenomics
  • 3.3 Metagenomics
  • 3.4 Transcriptomics
  • 3.5 Epitranscriptomics
  • 4. Specific omics datasets based on MS approach
  • 4.1 Proteomics
  • 4.2 Epiproteomics
  • 4.3 Metabolomics
  • 4.4 Glycomics
  • 4.5 Lipidomics.
  • 5. Specific omics datasets based on knowledge
  • 5.1 Microbiomics
  • 5.2 Immunomics
  • 6. Integration of omics datasets
  • 6.1 Methods of integration of omics data
  • 6.2 Techniques used for integration of multiomics data
  • 6.2.1 Machine learning
  • 6.2.2 Deep learning and its application in types of omics data
  • 6.3 Biological tools and databases used in omics data analysis
  • 6.4 Challenges of integration of omics data
  • 6.5 Application of integrated omics data
  • References
  • 4
  • Systematic benchmarking of omics computational tools
  • 1. Introduction
  • 2. Methodology for setting up the benchmarking study
  • 2.1 Selection of reference model
  • 2.2 Construction of gold standard dataset
  • 2.3 Default parameters selection and optimization
  • 2.4 Selection of benchmarking datasets
  • 2.5 Selection of computational tools
  • 2.6 Computational efficiency and scalability
  • 2.7 Integration and interoperability
  • 3. Experimental setup
  • 3.1 QIAGEN Genomics Workbench
  • 3.2 Partek Genomics Suite
  • 3.3 Golden Helix
  • 3.4 Genomatix
  • 3.5 Biodatomics
  • 3.6 Basepair
  • 3.7 DNAnexus
  • 3.8 Lasergene Genomics Suite
  • 3.9 NextGENe
  • 4. Case studies
  • 4.1 Case study 1: Hybrid assembly strategy on genomics data analysis
  • 4.1.1 Data collection
  • 4.1.2 Genome assembly
  • 4.1.3 Scaffolding
  • 4.1.4 Metrics for quality control
  • 4.1.5 Genome consistency plots
  • 4.2 Case study 2: Computational cost analysis by assessing Oxford nanopore read assemblers
  • 4.3 Case study 3: Genome assembly methods on metagenomic sequencing data
  • 4.3.1 Metagenome assembly
  • 4.3.2 Contig statistics
  • 4.3.3 Contig binning and MAG qualities
  • 4.3.4 Annotate MAGs into species
  • 4.4 Case study 4: Data-independent acquisition mass spectrometry for immunopeptidomics
  • 4.4.1 Library search-based DIA data analysis.
  • 4.4.2 Software tools for peptide sequence and statistical data analysis
  • 4.5 Case study 5: Long-read RNA-sequencing analysis tools using in silico mixtures
  • 4.5.1 Long-read isoform detection
  • 4.5.2 Transcript-level quantification of detected isoforms
  • 4.5.3 Read count processing
  • 4.5.4 Transcriptomic alignment
  • 4.5.5 Differential transcript expression and usage analysis
  • 5. The future of benchmarking challenges
  • 6. Conclusion
  • 7. Tools for omics data analysis
  • References
  • 5
  • Pharmacogenomics, nutrigenomics, and microbial omics
  • 1. Introduction
  • 2. Pharmacogenomics
  • 2.1 Why pharmacogenomics?
  • 2.2 Discovery of pharmacogenomics
  • 2.2.1 Cholinesterase inhibitors
  • 2.2.2 Memantine
  • 2.2.3 BACE inhibitors
  • 2.3 The promise of pharmacogenomics
  • 2.3.1 Personalized medicine
  • 2.3.2 Drug selection and dosing
  • 2.3.3 Adverse drug reactions
  • 2.3.4 Drug development and clinical trials
  • 2.3.5 Cost-effectiveness
  • 2.4 Pharmacogenomics as a powerful tool
  • 2.4.1 Improving the safety and effectiveness of medications
  • 2.4.2 Reducing health-care costs
  • 2.4.3 Improving the accuracy of clinical guidelines and treatment recommendations
  • 2.4.4 Enhancing the understanding of the underlying causes of diseases
  • 2.5 Pharmacogenomics-A solution
  • 2.6 Role of pharmacogenomics in drug development
  • 2.7 Research scopes in pharmacogenomics
  • 2.7.1 Identifying genetic predictors of drug response
  • 2.7.2 Investigating the role of genetic variation in adverse drug reactions
  • 2.7.3 Exploring the use of pharmacogenomics in personalized medicine
  • 2.7.4 Improving drug development and regulatory processes
  • 3. Nutrigenomics
  • 3.1 Why nutrigenomics?
  • 3.2 Discovery of nutrigenomics
  • 3.3 The promise of nutrigenomics
  • 3.4 Nutrigenomics as a powerful tool
  • 3.4.1 Personalized dietary recommendations.
  • 3.4.2 Gene-nutrient interactions
  • 3.4.3 Chronic disease prevention and management
  • 3.4.4 Ethical considerations and challenges
  • 3.5 Nutrigenomics as a solution
  • 4. Microbial omics
  • 4.1 Why microbial omics?
  • 4.1.1 Metagenomics
  • 4.1.2 Metatranscriptomics
  • 4.1.3 Metaproteomics
  • 4.1.4 Metabolomics
  • 4.2 Discovery of microbial omics
  • 4.2.1 Genomics
  • 4.2.2 Metagenomics Fig. 5.2
  • 4.2.3 Transcriptomics
  • 4.2.4 Proteomics
  • 4.2.5 Metabolomics
  • 4.3 Promise of microbial omics
  • 4.3.1 Genomics
  • 4.3.2 Metagenomics
  • 4.3.3 Transcriptomics
  • 4.3.4 Proteomics
  • 4.3.5 Metabolomics
  • 5. Correlation between nutrigenomics, pharmacogenomics, and microbial omics
  • References
  • 6
  • Proteomics: Present and future prospective
  • 1. Introduction
  • 2. Label-free quantitative proteomics
  • 2.1 Relative quantification by peak intensity of LCMS
  • 2.2 Relative quantification by spectral count
  • 2.3 Absolute label-free quantification
  • 2.4 Commercially available software for label-free quantitative proteomics
  • 3. Techniques used in proteomics
  • 3.1 Isotope coded affinity tag (ICAT) labeling
  • 3.2 Stable isotope labeling with amino acids in cell culture (SILAC)
  • 3.3 Isobaric tag for relative and absolute quantitation (iTRAQ)
  • 3.4 2D gel electrophoresis
  • 3.5 2D differential gel electrophoresis
  • 3.6 Protein microarray
  • 3.7 Reverse phased protein microarray
  • 3.8 Mass spectrometry
  • 3.9 LCMS/MS
  • 3.10 MALDI TOF/TOF
  • 3.11 NMR spectroscopy
  • 4. Present prospective of proteomics
  • 5. Future prospective of proteomics
  • 6. Advance tools used for proteomics
  • 7. Conclusion
  • References
  • 7
  • Foodomics: Integrated omics for the food and nutrition science
  • 1. Introduction
  • 2. Major four areas of omics that are involved in foodomics are
  • 2.1 Genomics
  • 2.1.1 Nutritional genomics.