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BlueGnome Limited cytochip v2.0 microarray
Schematic illustration of chromosome 10 displaying the deletions at 10p12p11 in patients 1–6 and patient by Shadadpuri et al5 detected by <t>microarray</t> using the Ensembl browser. Deleted regions for the respective cases are shown as black bars. Smallest region of overlap (SRO) is indicated by vertical dotted lines. Positions are according to NCBI36 (hg18).
Cytochip V2.0 Microarray, 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/microarray+hybridization+solution+version+2/cytochip+oligo+array/pmc03179368-97-15-18
Average 90 stars, based on 1 article reviews
cytochip v2.0 microarray - by Bioz Stars, 2026-10
90/100 stars

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1) Product Images from "Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11"

Article Title: Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11

Journal: European Journal of Human Genetics

doi: 10.1038/ejhg.2011.71

Schematic illustration of chromosome 10 displaying the deletions at 10p12p11 in patients 1–6 and patient by Shadadpuri et al5 detected by microarray using the Ensembl browser. Deleted regions for the respective cases are shown as black bars. Smallest region of overlap (SRO) is indicated by vertical dotted lines. Positions are according to NCBI36 (hg18).
Figure Legend Snippet: Schematic illustration of chromosome 10 displaying the deletions at 10p12p11 in patients 1–6 and patient by Shadadpuri et al5 detected by microarray using the Ensembl browser. Deleted regions for the respective cases are shown as black bars. Smallest region of overlap (SRO) is indicated by vertical dotted lines. Positions are according to NCBI36 (hg18).

Techniques Used: Microarray

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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).

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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

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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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