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Oxford Gene Technology 4 × 180k custom oligonucleotide microarray
4 × 180k Custom Oligonucleotide Microarray, supplied by Oxford Gene Technology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/180k+oligonucleotide+microarray/60k+cytosure+constitutional+v3+microarray/pmc08854775-62-3-20
Average 90 stars, based on 1 article reviews
4 × 180k custom oligonucleotide microarray - by Bioz Stars, 2026-10
90/100 stars

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Hybridization:

Article Title: Detection rates and residual risk for a postnatal diagnosis of an atypical chromosome aberration following combined first-trimester screening.
Article Snippet: .. 9,10 CMA was performed using an array-based comparative genomic hybridization platform, a 180K oligonucleotide array with evenly distributed whole-genome coverage (Oxford Gene Technology). .. Analysis of copy number variants (CNVs) was performed using the CytoSure Interpret Software (Oxford Gene Technology).

Article Title: Method of determining disease causality of genome mutations
Article Snippet: .. DNA extracted from peripheral blood was used to perform comparative genomic hybridization array (aCGH) analysis on a custom designed 4×180K oligonucleotide microarray platform (Oxford Gene Technology (OGT), Oxford, UK). ..

Article Title: Partial Monosomy 21 Mirrors Gene Expression of Trisomy 21 in a Patient-Derived Neuroepithelial Stem Cell Model
Article Snippet: .. A 4 × 180K custom oligonucleotide microarray was used for array comparative genomic hybridization (aCGH) performed on peripheral blood (AMADID:03103, Oxford Gene Technology, Begbroke, Oxfordshire, United Kingdom) as previously described ( ). ..

Microarray:

Article Title: Ventriculomegaly and cerebellar hypoplasia in a neonate with interstitial 11q 24 deletion in Jacobsen syndrome region
Article Snippet: .. Array CGH , Chr11:12,692,285‐134,938,470 (Hg 19) affirmetrix 743K SNP Platform (average resolution ~ 0.88 kb) , Chr11:127,217,775‐129, 666,990 (Hg 19) Human Genome CGH Microarray Kit G3 180 (average resolution ∼13 Kb) (Agilent Technologies) , Chr11:126,633,940‐132, 060,375 (Hg 18) Illumina Human 1 M(illumine, Inc, San Diego, California) , Chr11:125,780,310–128, 942,331 (Hg 19) Custom designed 4 × 180K oligonucleotide microarray (Oxford Gene Technology (OGT). , Chr11:126,767,670‐129, 667,131 (Hg 18) 4 × 44 K microarray platform (average resolution ∼75 Kb) (Agilent Technologies) , Chr11:120,476,074‐128, 148,010 (Hg 18) Affymetrix 500 K SNP Platform (average resolution ∼10 kb) or Agilent 44B platform (average resolution ∼75 kb), (Agilent Technologies , Chr11:124.29–129.03 (Hg 17) Spectral Genomics 1 Mb array (Spectral Genomics, Houston, TX). ..

Article Title: Method of determining disease causality of genome mutations
Article Snippet: .. DNA extracted from peripheral blood was used to perform comparative genomic hybridization array (aCGH) analysis on a custom designed 4×180K oligonucleotide microarray platform (Oxford Gene Technology (OGT), Oxford, UK). ..

Article Title: Evaluation of the ISL1 gene in the pathogenesis of bladder exstrophy in a Swedish cohort
Article Snippet: .. For array-CGH analysis, a 180K custom oligonucleotide microarray with whole-genome coverage and a median probe spacing of ~18 kb was used (Oxford Gene Technology, Yarnton, Oxfordshire, UK). ..

Article Title: Partial Monosomy 21 Mirrors Gene Expression of Trisomy 21 in a Patient-Derived Neuroepithelial Stem Cell Model
Article Snippet: .. A 4 × 180K custom oligonucleotide microarray was used for array comparative genomic hybridization (aCGH) performed on peripheral blood (AMADID:03103, Oxford Gene Technology, Begbroke, Oxfordshire, United Kingdom) as previously described ( ). ..

Article Title: Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization
Article Snippet: .. In 13 cases (P2046_133, P2109_123, P2109_150, P2109_151, P2109_162, P2109_188, P2109_190, P2109_302, P4855_511, P4855_512, P2109_176, P1426_301, P2109_185), the CMA was performed with an 180K custom oligonucleotide microarray with whole genome coverage and a median resolution of approximately 18 kb (Oxford Gene Technology (OGT), Oxfordshire, UK). ..

Article Title: From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability
Article Snippet: .. A 4 × 180K custom oligonucleotide microarray with whole-genome coverage and a median probe spacing of approximately 18 kb was used (AMADID:031035, Oxford Gene Technology, Begbroke, Oxfordshire, UK). ..



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Copy number status and fragment orientation as revealed by chromosomal  microarray  (CMA) and whole genome sequencing (WGS) of the complex rearrangements.

Journal: PLoS Genetics

Article Title: Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization

doi: 10.1371/journal.pgen.1007780

Figure Lengend Snippet: Copy number status and fragment orientation as revealed by chromosomal microarray (CMA) and whole genome sequencing (WGS) of the complex rearrangements.

Article Snippet: In 13 cases (P2046_133, P2109_123, P2109_150, P2109_151, P2109_162, P2109_188, P2109_190, P2109_302, P4855_511, P4855_512, P2109_176, P1426_301, P2109_185), the CMA was performed with an 180K custom oligonucleotide microarray with whole genome coverage and a median resolution of approximately 18 kb (Oxford Gene Technology (OGT), Oxfordshire, UK).

Techniques: Microarray, Sequencing