Literature DB >> 15832308

BAC-based PCR fragment microarray: high-resolution detection of chromosomal deletion and duplication breakpoints.

Hua Ren1, Wendy Francis, Amber Boys, Anderly C Chueh, Nick Wong, Phung La, Lee H Wong, Jacinta Ryan, Howard R Slater, K H Andy Choo.   

Abstract

The introduction of molecular techniques in conjunction with classical cytogenetic methods has in recent years greatly improved the diagnostic potential for chromosomal abnormalities. In particular, microarray-comparative genomic hybridization (CGH) based on the use of BAC clones promises a sensitive strategy for the detection of DNA copy-number changes on a genomewide scale, offering a resolution as high as >30,000 "bands" (as defined by the number of BACs within the currently highest-density BAC array) [Ishkanian et al., 2004]. We have tested the possibility of further increasing this resolution using PCR fragments generated from individual BAC clones. Using this approach, we have efficiently defined the proximal and distal breakpoints in two cytogenetic cases, one duplication and one deletion, to within 5-20 kb. The results support the potential use of BAC-based PCR fragments to further improve the resolution of the microarray-CGH strategy by an order of magnitude.

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Year:  2005        PMID: 15832308     DOI: 10.1002/humu.20164

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  6 in total

1.  High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs.

Authors:  Howard R Slater; Dione K Bailey; Hua Ren; Manqiu Cao; Katrina Bell; Steven Nasioulas; Robert Henke; K H Andy Choo; Giulia C Kennedy
Journal:  Am J Hum Genet       Date:  2005-09-16       Impact factor: 11.025

2.  Investigation of a patient with a partial trisomy 16q including the fat mass and obesity associated gene (FTO): fine mapping and FTO gene expression study.

Authors:  Linda van den Berg; Henriette Delemarre-van de Waal; Joan C Han; Bauke Ylstra; Paul Eijk; Maria Nesterova; Peter Heutink; Constantine A Stratakis
Journal:  Am J Med Genet A       Date:  2010-03       Impact factor: 2.802

3.  Novel duplication on chromosome 16 (q12.1-q21) associated with behavioral disorder, mild cognitive impairment, speech delay, and dysmorphic features: case report.

Authors:  Ljubica Odak; Ingeborg Barisić; Leona Morozin Pohovski; Mariluce Riegel; Albert Schinzel
Journal:  Croat Med J       Date:  2011-06       Impact factor: 1.351

4.  Human and mouse oligonucleotide-based array CGH.

Authors:  Paul van den Ijssel; Marianne Tijssen; Suet-Feung Chin; Paul Eijk; Beatriz Carvalho; Erik Hopmans; Henne Holstege; Dhinoth Kumar Bangarusamy; Jos Jonkers; Gerrit A Meijer; Carlos Caldas; Bauke Ylstra
Journal:  Nucleic Acids Res       Date:  2005-12-16       Impact factor: 16.971

5.  Tetralogy of Fallot and Hypoplastic Left Heart Syndrome - Complex Clinical Phenotypes Meet Complex Genetic Networks.

Authors:  Harald Lahm; Patric Schön; Stefanie Doppler; Martina Dreßen; Julie Cleuziou; Marcus-André Deutsch; Peter Ewert; Rüdiger Lange; Markus Krane
Journal:  Curr Genomics       Date:  2015-06       Impact factor: 2.236

6.  Progenetix: 12 years of oncogenomic data curation.

Authors:  Haoyang Cai; Nitin Kumar; Ni Ai; Saumya Gupta; Prisni Rath; Michael Baudis
Journal:  Nucleic Acids Res       Date:  2013-11-12       Impact factor: 16.971

  6 in total

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