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blue-fuse for bac and 4x44k oligo-microarrays software package  (BlueGnome Limited)

 
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    Structured Review

    BlueGnome Limited blue-fuse for bac and 4x44k oligo-microarrays software package
    Blue Fuse For Bac And 4x44k Oligo Microarrays Software Package, 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/bac+microarray/cytochip+isca+4x44k+v1+0/pm34338393-52-7-13
    Average 90 stars, based on 1 article reviews
    blue-fuse for bac and 4x44k oligo-microarrays software package - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Clinical impact of copy number variation changes in bladder cancer samples.
    Article Snippet: Two independent platforms were used for the detection of genomic imbalances: i) CytoChip ISCA 4x44K v1.0 (BlueGnome), scanned with an Agilent G2505 microarray scanner (Agilent Technologies, Inc.) and analysed by BlueFuse Multi v3.1 (Illumina, Inc.) and ii) Infinium OncoArray‐500K BeadChip (Illumina, Inc.), scanned with iScan (Illumina, Inc.) and analysed using KaryoStudio v.1.4 (Illumina, Inc.).

    Article Title: Clinical impact of copy number variation changes in bladder cancer samples
    Article Snippet: Two independent platforms were used for the detection of genomic imbalances: i) CytoChip ISCA 4x44K v1.0 (BlueGnome), scanned with an Agilent G2505 microarray scanner (Agilent Technologies, Inc.) and analysed by BlueFuse Multi v3.1 (Illumina, Inc.) and ii) Infinium OncoArray-500K BeadChip (Illumina, Inc.), scanned with iScan (Illumina, Inc.) and analysed using KaryoStudio v.1.4 (Illumina, Inc.).

    Article Title: Multiplex Proteomic Evaluation in Inborn Errors with Deregulated IgE Response.
    Article Snippet: Genomic Hybridization Microarray (Array–CGH) Analysis Based on the presence of multiple congenital anomalies and dysmorphisms, a comparative genomic hybridization microarray (Array–CGH) analysis using the CytoChip oligo–array ISCA 4X44K resolution (BlueGnome, Cambridge, UK) was performed according to the recommendations of the manufacturer.

    Article Title: Multiplex Proteomic Evaluation in Inborn Errors with Deregulated IgE Response
    Article Snippet: Based on the presence of multiple congenital anomalies and dysmorphisms, a comparative genomic hybridization microarray (Array–CGH) analysis using the CytoChip oligo–array ISCA 4X44K resolution (BlueGnome, Cambridge, UK) was performed according to the recommendations of the manufacturer.

    BAC Assay:

    Article Title: A 343 Italian cohort of patients analysed with array-comparative genomic hybridization: unsolved problems and genetic counselling difficulties.
    Article Snippet: Background The recent introduction of microarrays for genetic analyses has allowed higher etiological diagnostic rates in patient with intellectual disability (ID), autism spectrum disorders (ASD), epilepsy and multiple congenital anomalies (MCA), because of its resolution.. This approach still results of high complexity and some limitations have been reported.. In fact, it discloses several variants of unknown significance (VOUS) or incidental findings.

    Software:

    Article Title: A 343 Italian cohort of patients analysed with array-comparative genomic hybridization: unsolved problems and genetic counselling difficulties.
    Article Snippet: Background The recent introduction of microarrays for genetic analyses has allowed higher etiological diagnostic rates in patient with intellectual disability (ID), autism spectrum disorders (ASD), epilepsy and multiple congenital anomalies (MCA), because of its resolution.. This approach still results of high complexity and some limitations have been reported.. In fact, it discloses several variants of unknown significance (VOUS) or incidental findings.

    Microarray:

    Article Title: Improving risk-stratification of patients with chronic lymphocytic leukemia using multivariate patient similarity networks.
    Article Snippet: Background: Better risk-stratification of patients with chronic lymphocytic leukemia (CLL) and identification of subsets of ultra-high-risk (HR)-CLL patients are crucial in the contemporary era of an expanded therapeutic armamentarium for CLL.. Methods: A multivariate patient similarity network and clustering was applied to assess the prognostic values of routine genetic, laboratory, and clinical factors and to identify subsets of ultra-HR-CLL patients.. The study cohort consisted of 116 HR-CLL patients (F/M 36/80, median age 63 yrs) carrying del(11q), del(17p)/TP53 mutations and/or complex karyotype (CK) at the time of diagnosis.



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    Image Search Results


    Human BACs and normal HPAEpiCs express cholinergic proteins. A, ELISA assays show that human BAC cell lines and HPAEpiCs express multiple nAChR subunits. The assay was completed in duplicate, and the whole experiment was carried out 2 independent times. Results indicated by a different letter are significantly different (P < 0.05). B, HPAEpiCs and human BACs express AChE, ChAT, CHT1, and VAChT. H520 human SCC-L cells were used as the positive control for the experiments outlined in A and B. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was used as the loading control, and the results were quantitated by densitometric analysis. The experiment was repeated twice, and the representative data are shown. C and D, immunohistochemistry of the human BAC microarray showed that BAC tumors (isolated from patients) express ChAT and VAChT in the cytoplasm, adjacent to the hematoxylin-counterstained dark nuclei in the tissue samples. A tumor microarray containing 81 cores of human BACs was used for these experiments and 4 panels of representative photos are shown. Scale bar, 20 μm.

    Journal: Cancer research

    Article Title: Inhibition of Cholinergic Signaling Causes Apoptosis in Human Bronchioalveolar Carcinoma

    doi: 10.1158/0008-5472.CAN-12-3190

    Figure Lengend Snippet: Human BACs and normal HPAEpiCs express cholinergic proteins. A, ELISA assays show that human BAC cell lines and HPAEpiCs express multiple nAChR subunits. The assay was completed in duplicate, and the whole experiment was carried out 2 independent times. Results indicated by a different letter are significantly different (P < 0.05). B, HPAEpiCs and human BACs express AChE, ChAT, CHT1, and VAChT. H520 human SCC-L cells were used as the positive control for the experiments outlined in A and B. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was used as the loading control, and the results were quantitated by densitometric analysis. The experiment was repeated twice, and the representative data are shown. C and D, immunohistochemistry of the human BAC microarray showed that BAC tumors (isolated from patients) express ChAT and VAChT in the cytoplasm, adjacent to the hematoxylin-counterstained dark nuclei in the tissue samples. A tumor microarray containing 81 cores of human BACs was used for these experiments and 4 panels of representative photos are shown. Scale bar, 20 μm.

    Article Snippet: Human BAC tissue microarray (TMA) slides (Abnova) were deparaffinized and rehydrated as described previously ( 19 , 20 ).

    Techniques: Enzyme-linked Immunosorbent Assay, Positive Control, Control, Immunohistochemistry, Microarray, Isolation