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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Detalhes bibliográficos
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.
Formato: Artigo
Idioma:Inglês
Publicado em: Association of Biomolecular Resource Facilities 2009
Assuntos:
ABRF 2009 Selected Presentations
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2777346/
https://ncbi.nlm.nih.gov/pubmed/19949697
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