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...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Hauptverfasser: 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.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Association of Biomolecular Resource Facilities 2009
Schlagworte:
ABRF 2009 Selected Presentations
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2777346/
https://ncbi.nlm.nih.gov/pubmed/19949697
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