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J Biomol Tech ; 20(5): 253-7, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19949697

ABSTRACT

Identifying genetic variants and mutations that underlie human diseases requires development of robust, cost-effective tools for routine resequencing of regions of interest in the human genome. Here, we demonstrate that coupling Applied Biosystems SOLiD system-sequencing platform with microarray capture of targeted regions provides an efficient and robust method for high-coverage resequencing and polymorphism discovery in human protein-coding exons.


Subject(s)
Polymorphism, Genetic , Sequence Analysis, DNA/methods , Base Sequence , Biomedical Technology/methods , Exons , Genetic Variation , Genome, Human , Heterozygote , Homozygote , Humans , Molecular Sequence Data , Mutation , Oligonucleotide Array Sequence Analysis
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