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Springer Gene Regulatory Sequences and Human Disease

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Description

This book reviews breakthroughs in genomics that have led to new understanding of the effect of gene regulatory sequences in disease. Includes examples of nucleotide variants in noncoding sequences that have been shown to be associated with human diseases. From the Back Cover Genes make up less than 2% of our DNA and within the remaining 98% lie other extremely important sequences that function as gene regulatory elements, instructing genes when, where and at what levels to turn on or off. In this book, we introduce the different types of gene regulatory elements and how to identify and functionally characterize them. In addition, we describe several pioneering examples of how mutations in these elements have been found to cause human disease.With advances in DNA sequencing, the ability to identify disease-associated mutations in these regulatory elements is rapidly increasing. This book provides a great starting point for clinicians, geneticists, genomicists, developmental biologists and computational biologists to understand how to identify gene regulatory elements and associate nucleotide variation within them to human disease.

Product Specifications

Format
paperback
Domain
Amazon UK
Publication Date
11 June 2014
Listed Since
11 June 2014

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