Next-generation DNA and RNA sequencing has revolutionized biology and medicine. With sequencing cost continuously dropping and our ability to generate large datasets rising, data analysis becomes more important than ever. Next-Generation Sequencing Data Analysis walks readers through NGS data analysis step-by-step for a wide range of NGS applications.
For each NGS application, this book covers topics from experimental design, sample processing, sequencing strategy formulation, to sequencing reads quality control, data preprocessing, reads mapping or assembly, and more advanced stages that are specific to each application. Major applications include:
RNA-seq: both bulk and single-cell (separate chapters)
Genotyping and variant discovery through whole genome/exome sequencing
Clinical sequencing and detection of actionable variants
De novo genome assembly
ChIP-seq to map protein-DNA interactions
Epigenomics through DNA methylation sequencing
Metagenome sequencing for microbiome analysis
Before detailing the analytic steps for each of these applications, the book presents introductory cellular and molecular biology as a refresher mostly for data scientists, the ins and outs of widely used NGS platforms, and an overview of computing needs for NGS data management and analysis. The book concludes with a chapter on the changing landscape of NGS technologies and data analytics.
The second edition of this book builds on the well-received first edition by providing updates to each chapter. Two brand new chapters are added to meet rising data analysis demands on single-cell RNA-seq and clinical sequencing. The increasing use of long-reads sequencing has also been reflected in all NGS applications. This book discusses concepts and principles that underlie each analytic step, along with software tools for implementation. It highlights key features of the tools while omitting tedious details to provide an easy-to-follow guide for practitioners in life sciences, bioinformatics, biostatistics, and data science. Tools introduced in this book are open-source and freely available.
For each NGS application, this book covers topics from experimental design, sample processing, sequencing strategy formulation, to sequencing reads quality control, data preprocessing, reads mapping or assembly, and more advanced stages that are specific to each application. Major applications include:
RNA-seq: both bulk and single-cell (separate chapters)
Genotyping and variant discovery through whole genome/exome sequencing
Clinical sequencing and detection of actionable variants
De novo genome assembly
ChIP-seq to map protein-DNA interactions
Epigenomics through DNA methylation sequencing
Metagenome sequencing for microbiome analysis
Before detailing the analytic steps for each of these applications, the book presents introductory cellular and molecular biology as a refresher mostly for data scientists, the ins and outs of widely used NGS platforms, and an overview of computing needs for NGS data management and analysis. The book concludes with a chapter on the changing landscape of NGS technologies and data analytics.
The second edition of this book builds on the well-received first edition by providing updates to each chapter. Two brand new chapters are added to meet rising data analysis demands on single-cell RNA-seq and clinical sequencing. The increasing use of long-reads sequencing has also been reflected in all NGS applications. This book discusses concepts and principles that underlie each analytic step, along with software tools for implementation. It highlights key features of the tools while omitting tedious details to provide an easy-to-follow guide for practitioners in life sciences, bioinformatics, biostatistics, and data science. Tools introduced in this book are open-source and freely available.
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