chromosomal microarray analysis (cma) (Illumina Inc)

Illumina Inc is a verified supplier

About

News

Press Release

Team

Advisors

Partners

Contact

Bioz Stars

Bioz vStars

Buy from Supplier

Structured Review

Illumina Inc chromosomal microarray analysis (cma)
Chromosomal Microarray Analysis (Cma), supplied by Illumina 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/chromosomal+microarray+analysis+cma/chromosomal+microarray+analysis/pm39595626-56-9-18
Average 90 stars, based on 1 article reviews

chromosomal microarray analysis (cma) - by Bioz Stars, 2026-09

90/100 stars

Images

Microarray:

Article Title: Abstracts of the 12th European Cytogenomics Conference 2019
Article Snippet: .. Chromosomal microarray analysis (CMA, HumanCytoSNP-12 BeadChip, Illumina Inc.) revealed a ~7.9 Mb mosaic duplication of 2q11.1q12.1 material. ..

Article Title: Characterization of a Rare Mosaic Unbalanced Translocation of t(3;12) in a Patient With Neurodevelopmental Disorders
Article Snippet: .. Methods Genomic SNP chromosomal microarray analysis (SNP-CMA) was performed using DNA isolated from uncultured peripheral blood and processed using the Illumina CtyoSNP-850v1.2 BeadChip Platform, which contains approximately 846,500 genome-wide markers. .. Data was analyzed using Genome Studio v2011.1 (Illumina Inc, San Diego, California).

Article Title: Copy Number Variants in Cardiac Channelopathies: Still a Missed Part in Routine Arrhythmic Diagnostics.
Article Snippet: .. Deletion of exon 3 of RYR2 was detected by Chromosomal Microarray Analysis (CMA), performed using Infinium CytoSNP-850K BeadChip (Illumina, San Diego, CA, USA), according to the manufacturer’s protocol. .. Array scanning data were generated on the Illumina NextSeq 550 system, and the results were analyzed by the BluefuseMulti 4.4 software.

Article Title: Complex genomic rearrangements of the Y chromosome in a premature infant.
Article Snippet: FISH images were captured using a Zeiss Axio Imager Z2 microscope and analysed using CytoVision Imaging Software (Leica Microsystems). .. Genomic SNP chromosomal microarray analysis (SNP-CMA) was completed using the Infinium Assay with the Illumina Infinium CytoSNP-850 K Beadchip Platform. .. The data was analysed using the Illumina Genome Studio Genotyping Module V3.2 (Illumina Inc).

Article Title: A heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome.
Article Snippet: Funding information Wellcome Trust.. Abstract Only a few individuals with 12q15 deletion have been described, presenting with a disorder characterized by learning disability, developmental delay, nasal speech, and hypothyroidism.. The smallest region of overlap for this syndrome was included in a genomic segment spanning CNOT2, KCNMB4, and PTPRB genes.

Article Title: A novel case of 16q22.3 duplication syndrome in a child with overgrowth: case report and literature review.
Article Snippet: .. According to standard procedures, Chromosomal Microarray Analysis (CMA) was performed on DNA extracted from peripheral blood using Infinium CytoSNP-850 K BeadChip (Illumina, San Diego, California) at an average resolution of 100 kb. .. Array scanning data were generated by the NextSeq 550 system (Illumina) and results were analyzed by Bluefuse Multi software.

Isolation:

Genome Wide:

other:

Article Title: Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters.
Article Snippet: Results were interpreted using Illumina BlueFuse Multi software.

Article Title: Meeting abstracts from the 11th European Cytogenetics Conference
Article Snippet: Systematic screening for pathogenic mutations involved karyotyping, screening for fragile X syndrome, screening for metabolic disorders, targeted MLPA test with probemixes Telomeres 3 and 5, Microdeletion 1 and 2, Autism 1, MRX (MRC, Holland) and chromosomal microarray analysis (CMA) (Illumina or Affymetrix).

Review