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

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 ca...

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Main Authors: Antipova, Alena A., Sokolsky, Tanya D., Clouser, Christopher R., Dimalanta, Eileen T., Hendrickson, Cynthia L., Kosnopo, Cisilya, Lee, Clarence C., Ranade, Swati S., Zhang, Lei, Blanchard, Alan P., McKernan, Kevin J.
格式: Artigo
語言:Inglês
出版: Association of Biomolecular Resource Facilities 2009
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC2777346/
https://ncbi.nlm.nih.gov/pubmed/19949697
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