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oncoscan cna arrays  (Thermo Fisher)


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    Thermo Fisher oncoscan cna arrays
    OSCHP plots by Affymetrix <t>OncoScan</t> for whole‐genome <t>CNA.</t> (A) Genomic copy number gain and loss for chromosomes 1 to 22 and X were obtained in nine cases, with LM‐BN regions presented above and LMS regions below. Arrows indicate CNA shared by LM‐BN and LMS, indicating clonality. (Case 1 LM‐BN was tetraploid. A circular dot in case 2 indicates STUMP component.) (B, C) Dot plots represented the number of detectable sites of (B) CNA gain and (C) loss in genomic regions from nine cases. (D) Dot plots for LOH in LM‐BN and LMS. (E, F) Fraction of genome alteration in LMS and LM‐BN regions (E) individually and (F) combined analysis of fraction of genome alteration in LMS and LM‐BN. * p <0.05; ** p <0.01; *** p < 0.001; ns = no statistical significance.
    Oncoscan Cna Arrays, 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/oncoscan+array/pmc11717496-99-4-8
    Average 90 stars, based on 1 article reviews
    oncoscan cna arrays - by Bioz Stars, 2026-10
    90/100 stars

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    1) Product Images from "Genomic characterization and histologic analysis of uterine leiomyosarcoma arising from leiomyoma with bizarre nuclei"

    Article Title: Genomic characterization and histologic analysis of uterine leiomyosarcoma arising from leiomyoma with bizarre nuclei

    Journal: The Journal of Pathology

    doi: 10.1002/path.6379

    OSCHP plots by Affymetrix OncoScan for whole‐genome CNA. (A) Genomic copy number gain and loss for chromosomes 1 to 22 and X were obtained in nine cases, with LM‐BN regions presented above and LMS regions below. Arrows indicate CNA shared by LM‐BN and LMS, indicating clonality. (Case 1 LM‐BN was tetraploid. A circular dot in case 2 indicates STUMP component.) (B, C) Dot plots represented the number of detectable sites of (B) CNA gain and (C) loss in genomic regions from nine cases. (D) Dot plots for LOH in LM‐BN and LMS. (E, F) Fraction of genome alteration in LMS and LM‐BN regions (E) individually and (F) combined analysis of fraction of genome alteration in LMS and LM‐BN. * p <0.05; ** p <0.01; *** p < 0.001; ns = no statistical significance.
    Figure Legend Snippet: OSCHP plots by Affymetrix OncoScan for whole‐genome CNA. (A) Genomic copy number gain and loss for chromosomes 1 to 22 and X were obtained in nine cases, with LM‐BN regions presented above and LMS regions below. Arrows indicate CNA shared by LM‐BN and LMS, indicating clonality. (Case 1 LM‐BN was tetraploid. A circular dot in case 2 indicates STUMP component.) (B, C) Dot plots represented the number of detectable sites of (B) CNA gain and (C) loss in genomic regions from nine cases. (D) Dot plots for LOH in LM‐BN and LMS. (E, F) Fraction of genome alteration in LMS and LM‐BN regions (E) individually and (F) combined analysis of fraction of genome alteration in LMS and LM‐BN. * p <0.05; ** p <0.01; *** p < 0.001; ns = no statistical significance.

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    Related Articles

    other:

    Article Title: Genomic characterization and histologic analysis of uterine leiomyosarcoma arising from leiomyoma with bizarre nuclei
    Article Snippet: DNA was analyzed using Affymetrix OncoScan CNA arrays (Thermo Fisher Scientific, Santa Clara, CA, USA).



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    Image Search Results


    OSCHP plots by Affymetrix OncoScan for whole‐genome CNA. (A) Genomic copy number gain and loss for chromosomes 1 to 22 and X were obtained in nine cases, with LM‐BN regions presented above and LMS regions below. Arrows indicate CNA shared by LM‐BN and LMS, indicating clonality. (Case 1 LM‐BN was tetraploid. A circular dot in case 2 indicates STUMP component.) (B, C) Dot plots represented the number of detectable sites of (B) CNA gain and (C) loss in genomic regions from nine cases. (D) Dot plots for LOH in LM‐BN and LMS. (E, F) Fraction of genome alteration in LMS and LM‐BN regions (E) individually and (F) combined analysis of fraction of genome alteration in LMS and LM‐BN. * p <0.05; ** p <0.01; *** p < 0.001; ns = no statistical significance.

    Journal: The Journal of Pathology

    Article Title: Genomic characterization and histologic analysis of uterine leiomyosarcoma arising from leiomyoma with bizarre nuclei

    doi: 10.1002/path.6379

    Figure Lengend Snippet: OSCHP plots by Affymetrix OncoScan for whole‐genome CNA. (A) Genomic copy number gain and loss for chromosomes 1 to 22 and X were obtained in nine cases, with LM‐BN regions presented above and LMS regions below. Arrows indicate CNA shared by LM‐BN and LMS, indicating clonality. (Case 1 LM‐BN was tetraploid. A circular dot in case 2 indicates STUMP component.) (B, C) Dot plots represented the number of detectable sites of (B) CNA gain and (C) loss in genomic regions from nine cases. (D) Dot plots for LOH in LM‐BN and LMS. (E, F) Fraction of genome alteration in LMS and LM‐BN regions (E) individually and (F) combined analysis of fraction of genome alteration in LMS and LM‐BN. * p <0.05; ** p <0.01; *** p < 0.001; ns = no statistical significance.

    Article Snippet: DNA was analyzed using Affymetrix OncoScan CNA arrays (Thermo Fisher Scientific, Santa Clara, CA, USA).

    Techniques: