4 × 180k custom oligonucleotide microarray (Oxford Gene Technology)
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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
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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 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 Article Title: Partial Monosomy 21 Mirrors Gene Expression of Trisomy 21 in a Patient-Derived Neuroepithelial Stem Cell Model Article Snippet: .. A 4 × 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) 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 Article Title: Evaluation of the ISL1 gene in the pathogenesis of bladder exstrophy in a Swedish cohort Article Snippet: .. For array-CGH analysis, a Article Title: Partial Monosomy 21 Mirrors Gene Expression of Trisomy 21 in a Patient-Derived Neuroepithelial Stem Cell Model Article Snippet: .. A 4 × 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 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 × |
