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chromosomal microarray analysis  (Thermo Fisher)


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    Structured Review

    Thermo Fisher chromosomal microarray analysis
    Chromosomal Microarray Analysis, supplied by Thermo Fisher, 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/chromosome+microarray+analysis/chromosomal+microarray+analysis++cma+/pm39923644-38-0-8
    Average 90 stars, based on 1 article reviews
    chromosomal microarray analysis - by Bioz Stars, 2026-10
    90/100 stars

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    other:

    Article Title: Tumor-associated macrophages respond to chemotherapy by detrimental transcriptional reprogramming and suppressing stabilin-1 mediated clearance of EGF
    Article Snippet: Gene expression was evaluated using a Human Clariom S Assays microarray (Affymetrix, USA), Chromosome Analysis Suite 4.0 (ChAS, RRID : SCR_015626, Affymetrix, USA) and Transcriptome Analysis Console (TAC) 4.0 software (RRID : SCR_018718), respectively, were used to process the results of microchipping (bioinformatic analysis).

    Article Title: A novel microdeletion affecting the CETP gene raises HDL-associated cholesterol levels.
    Article Snippet: We describe a novel, inherited 16q13 microdeletion that removes cholesteryl ester transfer protein (CETP) and several nearby genes.. The proband was originally referred for severe childhood-onset obesity and moderate developmental delay, but his fasting lipid profile revealed relatively high levels of high density lipoprotein cholesterol (HDL-C) and relatively low levels of low density lipoprotein cholesterol (LDL-C) for age, despite his obesity.. Testing of first-degree relatives identified two other microdeletion carriers.

    Article Title: Combined fetal fraction to analyze the Z-score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18, and 21
    Article Snippet: Patients at high risk for NIPT were confirmed by karyotyping (G-band resolution 400 bands) or chromosome microarray analysis (CMA) (CytoScanTM 750 K, Affymetrix, USA).

    Article Title: Mitotic recombinatory evolution in acute leukemia.
    Article Snippet: A cohort of leukemia cases is presented with ancillary testing that includes microarray studies, karyotyping, FISH, and RNA sequencing to illustrate clonal evolution.. Common evolution etiology with each case is apparent homologous mitotic recombination (HMR).. The cohort includes: four cases of Pre Bcell acute lymphoblastic leukemia (B-ALL) with a single translocation derivative (19)t(1;19)(q23.3;p13.3), an acute myelogenous leukemia (AML) case with a paracentric inversion of 11q13.3q23 in both homologues confirmed as a rare KMT2A MAML2 gene fusion, and a transplant patient in AML relapse with a t(6;11)(6q27;q23) and evolution to an additional derivative 6 chromosome.

    Article Title: Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults
    Article Snippet: Results were analyzed using the Chromosome Analysis Suite 4.0 software 87 (Affymetrix Applied Biosystem Microarray, Thermo Fisher, Milan, Italy) and annotated 88 based on GRCh37 (hg19).

    Article Title: Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR Syndrome
    Article Snippet: Microarray-based copy number analysis was performed using the Chromosome Analysis Suite software version 4.0 (Thermo Fisher Scientific Inc., Waltham, MA, USA), and the results were presented on the International System for Human Cytogenomic Nomenclature 2020 (ISCN, 2020).

    Microarray:

    Article Title: ZDHHC9 X-linked intellectual disability: Clinical and molecular characterization.
    Article Snippet: Programa de P os-graduação em Ciências da Saúde, Universidade de Brasília, Brasília, Brazil Programa de P os-graduação em Ciências Médicas, Universidade de Brasília, Brasília, Brazil Hospital Universitário, Universidade de Brasília, Brasília, Brazil Departamento de Genética e Morfologia, Instituto de Ciências Biol ogicas, Universidade de Brasília, Brasília, Brazil Programa de P os-graduação em Biologia Animal, Universidade de Brasília, Brasília, Brazil Faculdade de Medicina, Universidade de Brasília, Brasília, Brazil

    Article Title: Copy number variants and fetal structural abnormalities in stillborn fetuses: a secondary analysis of the Stillbirth Collaborative Research Network study
    Article Snippet: .. DNA Samples were analyzed using the Affymetrix Genome Wide Human single nucleotide polymorphism (SNP) Array 6.0 and the Chromosome Analysis Suite, version 1.0.1, and the NetAffx annotation database, version 28 for microarray analysis (Affymetrix). ..

    Genome Wide:

    Article Title: Copy number variants and fetal structural abnormalities in stillborn fetuses: a secondary analysis of the Stillbirth Collaborative Research Network study
    Article Snippet: .. DNA Samples were analyzed using the Affymetrix Genome Wide Human single nucleotide polymorphism (SNP) Array 6.0 and the Chromosome Analysis Suite, version 1.0.1, and the NetAffx annotation database, version 28 for microarray analysis (Affymetrix). ..



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