Sequencing PCR-Amplified DNA in Lipoprotein and Cardiovascular Disease Research

Sanger sequencing genomic DNA
DOI: 10.1007/978-1-60327-369-5_6 Publication Date: 2013-08-02T14:47:42Z
ABSTRACT
The discovery of novel genetic variants and mutations in lipoprotein and cardiovascular disease research requires DNA sequencing. Large-scale genomics facilities will increasingly accomplish this with a combination of "next-generation" DNA sequencing methodologies. However, laboratories with limited access to these emerging technologies can still support focused genomic studies with the use of automated Sanger sequencing. Here, we describe two robust methods for medium-throughput DNA sequencing from PCR-amplified fragments of genomic DNA.
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