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custom-designed oligonucleotide microarray genomedx v5  (GenomeDx Inc)

 
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    GenomeDx Inc custom-designed oligonucleotide microarray genomedx v5
    Custom Designed Oligonucleotide Microarray Genomedx V5, supplied by GenomeDx Inc, 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/custom+designed+oligonucleotide+microarray+genomedx+v5/pmc12131107-31-10-14
    Average 90 stars, based on 1 article reviews
    custom-designed oligonucleotide microarray genomedx v5 - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Ring Chromosome 17 Syndrome—A Case Report and Discussion of Diagnostic Methods
    Article Snippet: Whole-genome comparative genomic hybridization (array comparative genomic hybridization [aCGH]) and genotype analysis (custom-designed oligonucleotide microarray—GenomeDX v5) performed on a blood sample showed a 1759 Mb arr[GRCh37] 17p13.3 (48,858–1,807,652)×1 deletion classified as pathogenic, and fluorescence in situ hybridization (FISH) analysis on parental samples using probes RP11–1061C17 (17p13.3) and RP11–1087N2 (17q25.3) revealed a normal hybridization pattern confirming the de novo nature of the deletion.

    Article Title: Ring Chromosome 17 Syndrome-A Case Report and Discussion of Diagnostic Methods.
    Article Snippet: Whole- genome comparative genomic hybridization (array comparative genomic hybridization [aCGH]) and genotype analysis (custom- designed oligonucleotide microarray—GenomeDX v5) performed on a blood sample showed a 1759 Mb arr[GRCh37] 17p13.3 (48,858- 1,807,652)x1 deletion classified as pathogenic, and fluorescence in situ hybridization (FISH) analysis on parental samples using probes RP11- 1061C17 (17p13.3) and RP11- 1087N2 (17q25.3) revealed a normal hybridization pattern confirming the de novo nature of the deletion.

    Article Title: Bone marrow transplantation reverses metabolic alterations in multiple sulfatase deficiency: a case series.
    Article Snippet: Molecular Chromosomal microarray Whole genome array-based comparative genomic hybridization (aCGH) and genotype analyses are performedon a custom-designed oligonucleotide microarray (GenomeDx v5).

    Article Title: Bone marrow transplantation reverses metabolic alterations in multiple sulfatase deficiency: a case series.
    Article Snippet: Whole genome array-based comparative genomic hybridization (aCGH) and genotype analyses are performedon a custom-designed oligonucleotide microarray (GenomeDx v5).

    Article Title: Hereditary Myoclonus Dystonia: A Novel SGCE Variant and Phenotype Including Intellectual Disability
    Article Snippet: This test is performed on a custom-designed oligonucleotide microarray (GenomeDx v5) and the design is based on human genome build GRCh37/UCSChg19 and contains approximately 118,000 probes that provide copy number data and 66,000 probes that generate genotype information through analysis of SNPs.

    Article Title: Bone marrow transplantation reverses metabolic alterations in multiple sulfatase deficiency: a case series
    Article Snippet: Whole genome array-based comparative genomic hybridization (aCGH) and genotype analyses are performed on a custom-designed oligonucleotide microarray (GenomeDx v5).

    Microarray:

    Article Title: Mosaic Trisomy 16 Associated with Left Lung Agenesis, Abnormal Left Arm, and Right Pulmonary Artery Stenosis: Expanding the Phenotype and Review of the Literature
    Article Snippet: .. The CMA on foreskin was performed on a custom designed oligonucleotide microarray (GenomeDx v5). ..

    Article Title: Mosaic Trisomy 16 Associated with Left Lung Agenesis, Abnormal Left Arm, and Right Pulmonary Artery Stenosis: Expanding the Phenotype and Review of the Literature
    Article Snippet: .. Given normal postnatal studies on blood, array CGH and SNP microarray (GenomeDx v5) with an average resolution of approximately 35kb was performed on foreskin tissue and identified a mosaic gain of the entire chromosome 16, arr(16) × 2–3, consistent with mosaic trisomy 16. ..



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