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Polymorphism Discovery in High-Throughput Resequenced Microarray-Enriched Human Genomic Loci

This paper is available in a repository.
This paper is available in a repository.

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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.