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array comparative genomic hybridisation (array-cgh 180k)  (Oxford Gene Technology)

 
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    Structured Review

    Oxford Gene Technology array comparative genomic hybridisation (array-cgh 180k)
    Array Comparative Genomic Hybridisation (Array Cgh 180k), 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/array+cgh/180+k+oligonucleotide+microarray/pmc12215207-68-9-16
    Average 90 stars, based on 1 article reviews
    array comparative genomic hybridisation (array-cgh 180k) - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Fluorescence in situ hybridization test for detection of endometrial carcinoma cells by non‐invasive vaginal swab
    Article Snippet: With the support of Oxford Gene Technology (OGT), we upgraded their standard CGH + SNP 4 × 180k array (1500‐KIE; design_0002 Additional POLE; 084718 ) with increased resolution in 13 genes, conspicuous in the molecular sub classification of endometrial cancer.

    Article Title: Fluorescence in situ hybridization test for detection of endometrial carcinoma cells by non-invasive vaginal swab.
    Article Snippet: With the support of Oxford Gene Technology (OGT), we upgraded their standard CGH + SNP 4 × 180k array (1500- KIE; design_0002 AdditionalPOLE; 084718) with increased resolution in 13 genes, conspicuous in the molecular sub classification of endometrial cancer.

    Article Title: Structural Variants in COL1A1 and COL1A2 in Osteogenesis Imperfecta.
    Article Snippet: Dosage abnormalities were initially detected using MLPA (probekit P271- B2 for COL1A1 and P272- B2 for COL1A2, MRC- Holland, Netherlands) and array- CGH (Oxford Gene Technology, UK).

    Hybridization:

    Article Title: Further characterization of NFIB-associated phenotypes: Report of two new individuals.
    Article Snippet: .. Array-comparative genomic hybridization (Array-CGH) CytoSure Oligo Arrays OGT-Oxford Gene Technology), performed elsewhere, showed a deletion of the short arm of a Chromosome 9 in the p23p22.3 region sizing 232 Kb, starting at 14.107.008 pb and ending at 14.339.185 pb (hg19) including most of the gene NFIB (Nuclear Factor I/B; NFIB, *600728). ..

    Article Title: Further characterization of NFIB ‐associated phenotypes: Report of two new individuals
    Article Snippet: .. Array‐comparative genomic hybridization (Array‐CGH) CytoSure Oligo Arrays OGT‐Oxford Gene Technology), performed elsewhere, showed a deletion of the short arm of a Chromosome 9 in the p23p22.3 region sizing ~232 Kb, starting at 14.107.008 pb and ending at 14.339.185 pb (hg19) including most of the gene NFIB (Nuclear Factor I/B; NFIB, *600728). ..

    Article Title: Genotypic and Phenotypic Characterization of Seven Individuals With Predicted Bone Morphogenetic Protein 2 (BMP2) Haploinsufficiency.
    Article Snippet: .. For larger deletions, validation and segregation were done using array comparative genomic hybridisation (array- CGH 180K) (AMADID:031035, Oxford Gene Technology, Begbroke, Oxfordshire, UK) at the department of Clinical Genetics and Genomics at Karolinska University Hospital [17]. ..

    Article Title: Genotypic and Phenotypic Characterization of Seven Individuals With Predicted Bone Morphogenetic Protein 2 ( BMP2 ) Haploinsufficiency
    Article Snippet: .. For larger deletions, validation and segregation were done using array comparative genomic hybridisation (array‐CGH 180K) (AMADID:031035, Oxford Gene Technology, Begbroke, Oxfordshire, UK) at the department of Clinical Genetics and Genomics at Karolinska University Hospital [ ]. ..

    Extraction:

    Article Title: Novel cellular systems unveil mucosal melanoma initiating cells and a role for PI3K/Akt/mTOR pathway in mucosal melanoma fitness.
    Article Snippet: Samples and references were labelled using the CytoSure Genomic DNA Labelling Kit (Oxford Gene Technology). .. The CytoSure Array 8 × 60 k CGH were scanned by Agilent Surescan C scanner with 2 μm resolution; features were extracted with Feature Extraction software and log2 ratio data were imported and analyzed by Cytosure Interpret Software 4.11.36 (Oxford Gene Technology) for the identification of copy number variation (CNV). ..

    Software:

    Article Title: Novel cellular systems unveil mucosal melanoma initiating cells and a role for PI3K/Akt/mTOR pathway in mucosal melanoma fitness.
    Article Snippet: Samples and references were labelled using the CytoSure Genomic DNA Labelling Kit (Oxford Gene Technology). .. The CytoSure Array 8 × 60 k CGH were scanned by Agilent Surescan C scanner with 2 μm resolution; features were extracted with Feature Extraction software and log2 ratio data were imported and analyzed by Cytosure Interpret Software 4.11.36 (Oxford Gene Technology) for the identification of copy number variation (CNV). ..

    Biomarker Discovery:

    Article Title: Genotypic and Phenotypic Characterization of Seven Individuals With Predicted Bone Morphogenetic Protein 2 (BMP2) Haploinsufficiency.
    Article Snippet: .. For larger deletions, validation and segregation were done using array comparative genomic hybridisation (array- CGH 180K) (AMADID:031035, Oxford Gene Technology, Begbroke, Oxfordshire, UK) at the department of Clinical Genetics and Genomics at Karolinska University Hospital [17]. ..

    Article Title: Genotypic and Phenotypic Characterization of Seven Individuals With Predicted Bone Morphogenetic Protein 2 ( BMP2 ) Haploinsufficiency
    Article Snippet: .. For larger deletions, validation and segregation were done using array comparative genomic hybridisation (array‐CGH 180K) (AMADID:031035, Oxford Gene Technology, Begbroke, Oxfordshire, UK) at the department of Clinical Genetics and Genomics at Karolinska University Hospital [ ]. ..



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