School of Medicine Publications and Presentations

Genomic studies of human populations: Resequencing approaches to the identification of human quantitative loci

Document Type

Book Chapter

Publication Date

1-1-2015

Abstract

In this chapter, we explore resequencing approaches to identify the quantitative loci in human populations. We will discuss why sequencing studies are optimal for variant discovery for common complex disease and how we go about localizing and identifying these causal variants. There are several different sequencing applications available to us today ranging from RNA sequencing to targeted genomic sequencing and extending to whole genome sequencing. We explore each of these applications and their individual utilities. Further, we explore studies of complex pedigrees compared to unrelated individuals, the two most common study designs used for human complex disease.

Comments

© 2015 Springer-Verlag Berlin Heidelberg

https://rdcu.be/d7GM0

First Page

289

Last Page

299

Publication Title

Genome Mapping and Genomics in Human and Non-Human Primates

DOI

10.1007/978-3-662-46306-2_16

Academic Level

faculty

Mentor/PI Department

Office of Human Genetics

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