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105k-oligonucleotide microarray cytosure syndrome plus v2  (Oxford Gene Technology)

 
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    Oxford Gene Technology 105k-oligonucleotide microarray cytosure syndrome plus v2
    105k Oligonucleotide Microarray Cytosure Syndrome Plus V2, 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/oligonucleotide+microarray/105k+oligonucleotide+microarray+cytosure+syndrome+plus+v2/pmc03464631-211-8-14
    Average 90 stars, based on 1 article reviews
    105k-oligonucleotide microarray cytosure syndrome plus v2 - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    other:

    Article Title: Defining the phenotype associated with microduplication reciprocal to Sotos syndrome microdeletion.
    Article Snippet: Defining the Phenotype Associated With Microduplication Reciprocal to Sotos Syndrome Microdeletion Francesca Novara, Franco Stanzial, Elena Rossi, Francesco Benedicenti, Francesca Inzana, Eleonora Di Gregorio, Alfredo Brusco, Jesper Graakjaer, Christina Fagerberg, Elga Belligni, Margherita Silengo, Orsetta Zuffardi, and Roberto Ciccone* Department of Molecular Medicine, University of Pavia, Pavia, Italy Department of Pediatrics, Genetic Counselling Service, Regional Hospital of Bolzano, Bolzano, Italy Department of Medical Sciences, University of Torino, Torino, Italy S.C.D.U.. Medical Genetics, Città della Salute e della Scienza, Torino, Italy Clinical Genetics Department, Vejle Hospital, Vejle, Denmark Clinical Genetics Department, Odense University Hospital, Odense, Denmark Department of Pediatrics, University of Turin, Turin, Italy Center for Genetic and Therapeutic Approaches, C. Mondino National Neurological Institute, Pavia, Italy

    Article Title: Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management
    Article Snippet: BAM files obtained from MPS of the validation data set of 296 NIPT samples is available to academic users upon request to the Data Access Committee of KU Leuven via the corresponding author (JRV).

    Article Title: Origins of Intraindividual Genetic Variation in Human Fetuses.
    Article Snippet: Background: Intraindividual copy number variation (CNV) origin is largely unknown.. They might be due to aging and/or common genome instability at the preimplantation stage while contribution of preimplantation in human intraindividual CNVs occurrence is unknown.. To address this question, we investigated mosaicism and its origin in the fetuses of natural conception.

    Hybridization:

    Article Title: Elevated α-synuclein levels inhibit mitophagic flux
    Article Snippet: For analysis of genomic identity by DNA fingerprinting, a reference set of 32 single nucleotide polymorphisms (SNPs) was analyzed with qPCR using TaqMan SNP Genotyping assays (Thermo Fisher) and TaqMan Genotyper software in the undifferentiated original control iPSC line (iPSC0028) and the undifferentiated iPSC0028 line in which the doxycycline-inducible extra SNCA copy had been introduced (Supplementary Fig. ). .. Karyotype analysis using array comparative genomic hybridization (aCGH) was performed with the CytoSure Syndrome Plus 60 K array (Oxford Gene Technology, UK), a platform that has genome-wide coverage with enrichment of target regions. .. Details of the array designs are available from Oxford Gene Technology ( http://www.ogt.co.uk/ ) or the authors.

    Genome Wide:

    Article Title: Elevated α-synuclein levels inhibit mitophagic flux
    Article Snippet: For analysis of genomic identity by DNA fingerprinting, a reference set of 32 single nucleotide polymorphisms (SNPs) was analyzed with qPCR using TaqMan SNP Genotyping assays (Thermo Fisher) and TaqMan Genotyper software in the undifferentiated original control iPSC line (iPSC0028) and the undifferentiated iPSC0028 line in which the doxycycline-inducible extra SNCA copy had been introduced (Supplementary Fig. ). .. Karyotype analysis using array comparative genomic hybridization (aCGH) was performed with the CytoSure Syndrome Plus 60 K array (Oxford Gene Technology, UK), a platform that has genome-wide coverage with enrichment of target regions. .. Details of the array designs are available from Oxford Gene Technology ( http://www.ogt.co.uk/ ) or the authors.

    Microarray:

    Article Title: Congenital diaphragmatic hernia as a part of Nance–Horan syndrome?
    Article Snippet: .. Chromosomal microarray analysis Copy number profiling was performed using Cytosure syndrome plus 8 × 60k arrays (Oxford Gene Technology- OGT, Oxford, UK) as previously described [ 21 ]. .. Chromosomal microarray analysis Copy number profiling was performed using Cytosure syndrome plus 8 × 60k arrays (Oxford Gene Technology- OGT, Oxford, UK) as previously described [ 21 ].

    Article Title: Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management
    Article Snippet: BAM files obtained from MPS of the validation data set of 296 NIPT samples is available to academic users upon request to the Data Access Committee of KU Leuven via the corresponding author (JRV). .. Array CGH (aCGH) analysis was performed as described previously 35 using either the 4x 180 K CytoSure Syndrome Plus Leuven Design microarray or the 8x 60 K CytoSure ISCA v2 microarray (AMADID 252721 and 020040, respectively; Oxford Gene Technology (OGT), Oxford, UK). .. Visualizations of results and data analysis were performed using the CytoSure Interpret Software (OGT) and with Cartagenia BENCH software (Cartagenia NV, Leuven, Belgium).



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