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BlueGnome Limited 180k isca cytochip
180k Isca Cytochip, supplied by BlueGnome Limited, 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/high-resolution+microarray+scanner/cytochip+oligo+array/pmc04244445-57-9-12
Average 90 stars, based on 1 article reviews
180k isca cytochip - by Bioz Stars, 2026-09
90/100 stars

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Article Title: A coalescence of two syndromes in a girl with terminal deletion and inverted duplication of chromosome 5
Article Snippet: Array-CGH was performed on DNA extracted from peripheral blood leukocytes of the patient and her parents using the BlueGnome CytoChip ISCA 8 × 60 K platform (BlueGnome Limited, Cambridge, United Kingdom).

Article Title: An improved method for genome wide DNA methylation profiling correlated to transcription and genomic instability in two breast cancer cell lines
Article Snippet: Briefly, CytoChip v2.0 (BlueGnome) with BAC clone human DNA fragments, representing the whole genome with 0.5-Mb resolution on average, was used to detect copy number variation (CNV) for both cell lines.

Article Title: Homozygous intronic variants in TPM2 cause recessively inherited Escobar variant of multiple pterygium syndrome and congenital myopathy.
Article Snippet: Please cite this article as: Schaida Schirwani , Anna Sarkozy , Rahul Phadke , Anne-Marie Childs , Rachael Mein , Azzam Ismail , Audrey Smith , Francesco Muntoni , Hobson Emma , Karen Pysden , Homozygous intronic variants in TPM2 cause recessively inherited Escobar variant of multiple pterygium syndrome and congenital myopathy, Neuromuscular Disorders (2020), doi: https://doi.org/10.1016/j.nmd.2020.09.033

Article Title: Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies
Article Snippet: To do so, the BlueGnome CytoChip ISCA 8×60 K v2.0 wholegenome oligo array was utilized for patients 1, 5, 9, 13, and 41.

MicroChIP Assay:

Article Title: Exploring Genetic Alterations in Hodgkin Lymphoma using Comparative Genomic Hybridization on DNA Microarrays
Article Snippet: .. For our analysis, we used the genomic array CytoChip (BlueGnome, Cambridge, UK), which is an oligonucleotide microchip with a density of 105.072 sequences covering the entire genome with a resolution of 35 Kb. ..



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Flow chart of microarray data analysis. The agilent single color microarray platform was used having more than 58,000 transcripts and further data processing was done using agilent GeneSpring software followed by pathway analysis using GSEA database. Numbers in parentheses illustrates number of pathways enriched in each category using GSEA database. DEGs-Differentially expressed genes, ANOVA-Analysis of variance, BP-Biological pathway, CC-Cellular component, MF-Molecular function.

Journal: bioRxiv

Article Title: Synovial fluid transcriptome dynamics in osteoarthritis progression: Implications in pathogenesis

doi: 10.1101/2024.06.24.600143

Figure Lengend Snippet: Flow chart of microarray data analysis. The agilent single color microarray platform was used having more than 58,000 transcripts and further data processing was done using agilent GeneSpring software followed by pathway analysis using GSEA database. Numbers in parentheses illustrates number of pathways enriched in each category using GSEA database. DEGs-Differentially expressed genes, ANOVA-Analysis of variance, BP-Biological pathway, CC-Cellular component, MF-Molecular function.

Article Snippet: Following hybridization, the array slides were washed and scanned with an Agilent SureScan High-Resolution DNA Microarray Scanner.

Techniques: Microarray, Software

The 11 genes were detected in the microarray analysis and in the human dataset. A correlation between FCs of genes. B heatmap with hierarchical clustering of FCs of the 11 genes commonly detected in the murine neurospheres and AD patients’ tissues

Journal: Cell & Bioscience

Article Title: Bradykinin promotes immune responses in differentiated embryonic neurospheres carrying APP swe and PS1 dE9 mutations

doi: 10.1186/s13578-024-01251-3

Figure Lengend Snippet: The 11 genes were detected in the microarray analysis and in the human dataset. A correlation between FCs of genes. B heatmap with hierarchical clustering of FCs of the 11 genes commonly detected in the murine neurospheres and AD patients’ tissues

Article Snippet: The arrays were then washed as described on Agilent SSPE wash protocol v. 2.1 and scanned with a High-Resolution Microarray Scanner (Agilent Technologies).

Techniques: Microarray