Reviewer: Pooja Sethi, MD (East Tennessee State University Quillen College of Medicine)
Description: Translational bioinformatics is defined as the development of storage-related, analytical, and interpretive methods to optimize the transformation of the increasing volume of biomedical data, and genomic data in particular, into proactive, predictive, preventive, and participatory health. This volume in the Translational Bioinformatics series introduces modern computational and statistical tools for translational epigenomic research with a special focus on DNA methylation.
Purpose: Over the past decade, epigenomics has emerged as a key area of molecular biology, epidemiology, and genome medicine. This book is as a powerful and integrative tool for understanding and translating discoveries and advances of genomic, transcriptomic, proteomic, and bioinformatics technologies into the study of human disease.
Audience: The book is aimed primarily at students, clinicians, and researchers with a basic background in bioinformatics and biostatistics who are interested in learning some key concepts in computational and statistical methods for analyzing epigenomic data.
Features: This book is edited by Dr. Andrew E. Teschendorff, a well-known figure in computational genomics. This series in translational bioinformatics focuses on articles/chapters presenting significant recent work in genomic, transcriptomic, proteomic, and bioinformatic profiles related to human organ or cell dysfunction and clinical findings. It includes bioinformatics-driven molecular and cellular disease mechanisms, the understanding of human diseases, and its use in the improvement of patient prognoses. Additionally, it provides practical and useful study insights into protocols of design and methodology. Topics covered in this book include normalization, correction for cellular heterogeneity, batch effects, clustering, supervised analysis, and integrative methods for stem epigenomics. The book is divided into two parts. The first part focuses on normalization and analysis methods for DNA methylation and ChIP-Seq data. The second past focuses on integrative and medical epigenomics. Chapters are uniformly formatted, and move from basic to more advanced concepts as the book progresses. The book includes color diagrams, bar graphs, and tables for easier understanding. In addition, chapters are well referenced for more extensive reading on the topic if readers so desire.
Assessment: This is a valuable resource for students, clinicians, and researchers who wish to understand the basics of modern computational and statistical tools for translational epigenomics research. The analytical, storage-related, and interpretive methods discussed in this book hold great promise in helping improve prediction, early diagnosis, severity monitoring, therapeutic effect, and prognosis of human diseases.
This volume in the Translational Bioinformatics series introduces modern computational and statistical tools for translational epigenomic research with a special focus on DNA methylation. … This is a valuable resource for students, clinicians, and researchers who wish to understand the basics of modern computational and statistical tools for translational epigenomics research. The analytical, storage-related, and interpretive methods discussed in this book hold great promise in helping improve prediction, early diagnosis, severity monitoring, therapeutic effect, and prognosis of human diseases.” (Pooja Sethi, Doody’s Book Reviews, July, 2015)