targeted 60k oligonucleotide microarray (GeneDx Inc)
90
Structured Review
GeneDx Inc
targeted 60k oligonucleotide microarray
![De novo 0.7 Mb deletion of chromosome 20q13.33 in the patient described here, ascertained with Illumina Omni1-Quad high-density single-nucleotide polymorphism (SNP) <t>microarray</t> platform, and visualized using GenomeStudio (v2009.2, www.Illumina.com ) genotyping module. The deletion is indicated by the arrow ; the corresponding chromosomal region is outlined in the ideogram below. The proband's microarray is uppermost; parental arrays of the same region are shown below the proband's. [Color figure can be viewed in the online issue, which is available at wileyonlinelibrary.com .]](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_3386/pmc03193386/pmc03193386__bdra0091-0862-f1.jpg)
Targeted 60k Oligonucleotide Microarray, supplied by GeneDx 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/genepix+pro+microarray+analysis+software/pmc03193386-35-5-13?v=GeneDx+Inc
Average 90 stars, based on 1 article reviews
Targeted 60k Oligonucleotide Microarray, supplied by GeneDx 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/genepix+pro+microarray+analysis+software/pmc03193386-35-5-13?v=GeneDx+Inc
Average 90 stars, based on 1 article reviews
targeted 60k oligonucleotide microarray - by Bioz Stars,
2026-08
90/100 stars
Images
1) Product Images from "De Novo Deletion of Chromosome 20q13.33 in a Patient with Tracheo-esophageal Fistula, Cardiac Defects and Genitourinary Anomalies Implicates GTPBP5 as a Candidate Gene"
Article Title: De Novo Deletion of Chromosome 20q13.33 in a Patient with Tracheo-esophageal Fistula, Cardiac Defects and Genitourinary Anomalies Implicates GTPBP5 as a Candidate Gene
Journal: Birth Defects Research. Part A, Clinical and Molecular Teratology
doi: 10.1002/bdra.20821
Figure Legend Snippet: De novo 0.7 Mb deletion of chromosome 20q13.33 in the patient described here, ascertained with Illumina Omni1-Quad high-density single-nucleotide polymorphism (SNP) microarray platform, and visualized using GenomeStudio (v2009.2, www.Illumina.com ) genotyping module. The deletion is indicated by the arrow ; the corresponding chromosomal region is outlined in the ideogram below. The proband's microarray is uppermost; parental arrays of the same region are shown below the proband's. [Color figure can be viewed in the online issue, which is available at wileyonlinelibrary.com .]
Techniques Used: Microarray