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custom 180k oligonucleotide microarray  (Agilent technologies)


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    Structured Review

    Agilent technologies custom 180k oligonucleotide microarray
    Custom 180k Oligonucleotide Microarray, supplied by Agilent technologies, 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/med_rxiv__2022__06__13__22276366-181-11-15
    Average 90 stars, based on 1 article reviews
    custom 180k oligonucleotide microarray - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    Microarray:

    Article Title: Pontocerebellar hypoplasia with rhombencephalosynapsis and microlissencephaly expands the spectrum of PCH type 1B.
    Article Snippet: .. Chromosomal analysis performed on amniotic fluid cells and based on 180K oligonucleotide microarray (Agilent Technologies, Les Ulis, France) revealed a normal male karyotype, 46, XY. ..

    Article Title: Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathy
    Article Snippet: .. Chromosomal microarray and copy number variant analysis A custom 180K oligonucleotide microarray (Agilent) was utilized for chromosomal microarray on a DNA sample from the older affected sibling, with a genome-wide functional resolution of 100 kilobases (kb). ..

    Article Title: Abstract Medizinische Genetik 2011
    Article Snippet: Aortic aneurysms are an important cause of mortality in the western world.. Monogenic disorders such as the Marfan syndrome (MFS) and the vascular type of Ehlers-Danlos syndrome (EDS) are good models for the study of the pathogenesis of aortic aneurysm.. In the MFS, progressive dilatation of the aortic root leads to aortic aneurysm and dissection, often associated with precocious death.

    Article Title: Microcephaly, short stature, and limb abnormality disorder due to novel autosomal biallelic DONSON mutations in two German siblings
    Article Snippet: .. Array-comparative genomic hybridization (CGH) analysis using a 180K oligonucleotide microarray (Agilent Technologies) was inconspicuous. ..

    Variant Assay:

    Article Title: Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathy
    Article Snippet: .. Chromosomal microarray and copy number variant analysis A custom 180K oligonucleotide microarray (Agilent) was utilized for chromosomal microarray on a DNA sample from the older affected sibling, with a genome-wide functional resolution of 100 kilobases (kb). ..

    Genome Wide:

    Article Title: Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathy
    Article Snippet: .. Chromosomal microarray and copy number variant analysis A custom 180K oligonucleotide microarray (Agilent) was utilized for chromosomal microarray on a DNA sample from the older affected sibling, with a genome-wide functional resolution of 100 kilobases (kb). ..

    Functional Assay:

    Article Title: Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathy
    Article Snippet: .. Chromosomal microarray and copy number variant analysis A custom 180K oligonucleotide microarray (Agilent) was utilized for chromosomal microarray on a DNA sample from the older affected sibling, with a genome-wide functional resolution of 100 kilobases (kb). ..

    Hybridization:

    Article Title: Abstract Medizinische Genetik 2011
    Article Snippet: Aortic aneurysms are an important cause of mortality in the western world.. Monogenic disorders such as the Marfan syndrome (MFS) and the vascular type of Ehlers-Danlos syndrome (EDS) are good models for the study of the pathogenesis of aortic aneurysm.. In the MFS, progressive dilatation of the aortic root leads to aortic aneurysm and dissection, often associated with precocious death.

    Article Title: Microcephaly, short stature, and limb abnormality disorder due to novel autosomal biallelic DONSON mutations in two German siblings
    Article Snippet: .. Array-comparative genomic hybridization (CGH) analysis using a 180K oligonucleotide microarray (Agilent Technologies) was inconspicuous. ..

    other:

    Article Title: Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathy
    Article Snippet: Three zebrafish embryos per micro-centrifuge tube were homogenized using a mortar and pestle (Fisher Scientific).



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    Image Search Results


    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