Targeted comparative genomic hybridization array for the detection of single- and multiexon gene deletions and duplications.
other · Level V
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- Record sourced from PubMed, PMID 19282776.
- Also identified by DOI 10.1097/GIM.0b013e318195e191.
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Abstract
To develop a high resolution microarray based method to detect single- and multiexons gene deletions and duplications. We have developed a high-resolution comparative genomic hybridization array to detect single- and multiexon deletions and duplications in a large set of genes on a single microarray, using the NimbleGen 385K array with an exon-centric design. We have successfully developed, validated, and implemented a targeted gene comparative genomic hybridization arrays for detecting single- and multiexon deletions and duplication in autosomal and X-linked disease-associated genes. The comparative genomic hybridization arrays can be adopted readily by clinical molecular diagnostic laboratories as a rapid, cost-effective, highly sensitive, and accurate approach for the detection of single- and multiexon deletions or duplications, particularly in cases where direct sequencing fails to identify a mutation.
Medical subject headings
- Comparative Genomic Hybridization
- DNA Mutational Analysis
- Gene Deletion
- Gene Duplication