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244k human genome cgh microarrays  (Agilent technologies)


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    Structured Review

    Agilent technologies 244k human genome cgh microarrays
    Genomic and transcriptomic evaluation of breast tumor patient-derived xenografts
    244k Human Genome Cgh Microarrays, supplied by Agilent technologies, 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/human+genome+cgh+microarray+244k/pmc03672825-11-45-47?v=Agilent+technologies
    Average 90 stars, based on 1 article reviews
    244k human genome cgh microarrays - by Bioz Stars, 2026-08
    90/100 stars

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    1) Product Images from "Patient-derived breast tumor xenografts facilitating personalized cancer therapy"

    Article Title: Patient-derived breast tumor xenografts facilitating personalized cancer therapy

    Journal: Breast Cancer Research : BCR

    doi: 10.1186/bcr3355

    Genomic and transcriptomic evaluation of breast tumor patient-derived xenografts
    Figure Legend Snippet: Genomic and transcriptomic evaluation of breast tumor patient-derived xenografts

    Techniques Used: Sequencing, Genome Wide, Microarray, Expressing



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    Image Search Results


    Genomic and transcriptomic evaluation of breast tumor patient-derived xenografts

    Journal: Breast Cancer Research : BCR

    Article Title: Patient-derived breast tumor xenografts facilitating personalized cancer therapy

    doi: 10.1186/bcr3355

    Figure Lengend Snippet: Genomic and transcriptomic evaluation of breast tumor patient-derived xenografts

    Article Snippet: Genomic , DNA copy number alterations: 14/18 pairs of tumors shared more than 56% copy number alterations, unsupervised hierarchical clustering showed 16/18 pairs segregated together. Recurrent changes between patient tumors and xenografts showed losses in 176 chromosomal regions and gains in 202 chromosomal regions , CGH array Agilent 244K human genome CGH microarrays. CGH results showed shared alterations between primary and xenograft tumors with more pronounced alterations in engrafted tumors, that is, TP53 patient 1 wild-type allele, xenograft LOH; ER+ tumor gained basal-like alterations , Paired-end sequencing to achieve deep coverage of patient blood, tumor, metastasis, and xenografted tumor Confirmed SNP coverage by Illumina 1M duo arrays. The PDX retained primary tumor mutations and showed enrichment of mutations similar to patient metastasis , Genome-wide SNPs with enhancement of existing aberrations , , .

    Techniques: Sequencing, Genome Wide, Microarray, Expressing