This cutting-edge reference book compiles standard operating procedures, protocols, and applications of next-generation sequencing (NGS). It discusses genomic testing applications through NGS. It pays special focus on the protocols for cataloguing variants of uncertain significance. Over the years, NGS and advanced bioinformatics approaches have allowed the transition of genomic assays into translational practices. The book covers visualisation of NGS datasets, investigation of early development impairment, and metagenome protocols. It also discusses the challenges in NGS methods.
Key Points:
Includes case studies of application of NGS in different taxa like humans, rodents, plants, and bacteria
Compiles protocols from various reputed companies like Illumina, PacBio, and ThermoFisher
Discusses the translational applications of NGS methods
Reviews machine learning heuristics for NGS data interpretation
Discusses emerging genomic assay technologies and characterising mechanisms of disease prevalence
The book is meant for researchers and industry experts in genomics, computational biology, and bioinformatics.
Chapter 7 and 9 of this book is freely available as a downloadable Open Access PDF at http://www.taylorfrancis.com under a Creative Commons [Attribution-Non Commercial-No Derivatives (CC BY-NC-ND)] 4.0 license.
Sprache
Verlagsort
Verlagsgruppe
Zielgruppe
Für höhere Schule und Studium
Für Beruf und Forschung
Academic, Postgraduate, and Professional
Illustrationen
6 s/w Abbildungen, 54 farbige Abbildungen, 6 s/w Zeichnungen, 54 farbige Zeichnungen, 35 s/w Tabellen
35 Tables, black and white; 54 Line drawings, color; 6 Line drawings, black and white; 54 Illustrations, color; 6 Illustrations, black and white
Maße
Höhe: 260 mm
Breite: 183 mm
Dicke: 21 mm
Gewicht
ISBN-13
978-1-032-39262-2 (9781032392622)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Klassifikation
Prashanth N Suravajhala is a Professor in the Systems Genomics Lab of the Department of Biosciences at Manipal University Jaipur. He has a PhD in Systems Biology from Aalborg University, Denmark. His group has benchmarked pipelines and developed methods for systems genomic integration. He is an Associate Editor of Frontiers in Genetics/Systems Biology, Bio-Protocol, Biomolecules, and BMC Medical Genomics.
Jeff W Bizzaro has been involved in the field of bioinformatics for more than 25 years and has made significant contributions to the development of bioinformatics software. He is a co-founder of Bioinformatics.org, a professional network that advocates for open science and provides various resources to students and professionals.
1. Technologies, Computations and Data Analysis for Next Generation Sequencing
2. Epigenetics: RNA-Seq, ChiP-Seq, MedIP-Seq and ATAC-Seq
3. Streamlining Next-Generation Sequencing Data Analysis with Nextflow and nf-core Pipelines
4. Best practices for variant calling using Genome Analysis Toolkit
5. Implementation of WGCNA for identifying regulatory modules in biological networks
6. Meta-analysis of RNA-seq and Microarray data
7. Best practices in single-cell RNA-seq data analysis
8. Integration of Spatial Transcriptomics and Single Cell RNA-Seq
9. Metagenomics Analysis Pipelines for Microbiome Studies: QIIME and Mothur
10. Standard Operating Procedure and Applications in Single-Cell Transcriptomics
11. Benchmarking and Evaluation of de novo Assembly Tools for Prokaryotic Long Reads from Oxford Nanopore Technologies
12. Best Practices for Reproducible of Microbial Genomics Analysis
13. Single Cell RNA-Seq Analyses in the Era of Artificial Intelligence
14. Towards single-molecule protein sequencing
15. SOPs on Effective Galaxy Workflows
16. Motif prediction using ChIP-Seq data analysis using Galaxy
17. Developing a Whole Exome Consensus Variant Calling Pipeline to Infer Causal Pathogenic Variants
Index
