Literature DB >> 19282776

Targeted comparative genomic hybridization array for the detection of single- and multiexon gene deletions and duplications.

Marwan K Tayeh1, Ephrem L H Chin, Vanessa R Miller, Lora J H Bean, Bradford Coffee, Madhuri Hegde.   

Abstract

PURPOSE: To develop a high resolution microarray based method to detect single- and multiexons gene deletions and duplications.
METHODS: 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.
RESULTS: 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.
CONCLUSION: 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.

Entities:  

Mesh:

Year:  2009        PMID: 19282776     DOI: 10.1097/GIM.0b013e318195e191

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  26 in total

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5.  Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes.

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Review 7.  Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns.

Authors:  Curtis R Coughlin; Gunter H Scharer; Tamim H Shaikh
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8.  Genetic screening for OPA1 and OPA3 mutations in patients with suspected inherited optic neuropathies.

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9.  Targeted polymerase chain reaction-based enrichment and next generation sequencing for diagnostic testing of congenital disorders of glycosylation.

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Journal:  Genet Med       Date:  2011-11       Impact factor: 8.822

10.  Copy Number Variation Disorders.

Authors:  Tamim H Shaikh
Journal:  Curr Genet Med Rep       Date:  2017-10-14
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