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array cgh analysis  (DNA Chip Research Inc)

 
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    DNA Chip Research Inc array cgh analysis
    Array <t>CGH</t> data of MYC and TP53 and TP53 sequencing data in early and advanced tubular adenocarcinomas of stomach . Early cancers are divided into intramucosal (m) cancers and submucosal (sm) cancers. Refer to Table 1 for sample numbers. Numerals are mean test/reference ratios of array CGH. Significant losses and gains are indicated with red and green, respectively. Wild type (wt) and mutation in exon (ex) and <t>intervening</t> <t>sequence</t> (IVS) of TP53 are indicated with yellow and gray, respectively.
    Array Cgh Analysis, supplied by DNA Chip Research Inc, 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/array+cgh+analysis/pmc02898698-215-27-6?v=DNA+Chip+Research+Inc
    Average 90 stars, based on 1 article reviews
    array cgh analysis - by Bioz Stars, 2026-07
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    Images

    1) Product Images from "Lineage analysis of early and advanced tubular adenocarcinomas of the stomach: continuous or discontinuous?"

    Article Title: Lineage analysis of early and advanced tubular adenocarcinomas of the stomach: continuous or discontinuous?

    Journal: BMC Cancer

    doi: 10.1186/1471-2407-10-311

    Array CGH data of MYC and TP53 and TP53 sequencing data in early and advanced tubular adenocarcinomas of stomach . Early cancers are divided into intramucosal (m) cancers and submucosal (sm) cancers. Refer to Table 1 for sample numbers. Numerals are mean test/reference ratios of array CGH. Significant losses and gains are indicated with red and green, respectively. Wild type (wt) and mutation in exon (ex) and intervening sequence (IVS) of TP53 are indicated with yellow and gray, respectively.
    Figure Legend Snippet: Array CGH data of MYC and TP53 and TP53 sequencing data in early and advanced tubular adenocarcinomas of stomach . Early cancers are divided into intramucosal (m) cancers and submucosal (sm) cancers. Refer to Table 1 for sample numbers. Numerals are mean test/reference ratios of array CGH. Significant losses and gains are indicated with red and green, respectively. Wild type (wt) and mutation in exon (ex) and intervening sequence (IVS) of TP53 are indicated with yellow and gray, respectively.

    Techniques Used: Sequencing, Mutagenesis

    Array CGH profiles . The chromosomal regions of copy number aberrations in the mucosal part of #S3 (S3m) are included basically in those in the invasive part (S3i), whereas those in the mucosal part of #A1 (A1m) are different from those of the invasive part (A1i).
    Figure Legend Snippet: Array CGH profiles . The chromosomal regions of copy number aberrations in the mucosal part of #S3 (S3m) are included basically in those in the invasive part (S3i), whereas those in the mucosal part of #A1 (A1m) are different from those of the invasive part (A1i).

    Techniques Used:



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    Image Search Results


    A) Result of array-CGH analysis of chromosome 2 with Agilent Human Genome CGH microarray Kit G3 400 in patient 1. The 1.914 Mb interstitial q37.1 deleted region of chromosome 2 extends between oligomers A_18_P13670199 (231,264,956 bp) and A_16_P00618306 (233,178,325 bp) flanked by oligomers A_16_P00615757 (231,257,468 bp) and A_16_P00618312 (233,181,399 bp) (UCSC Genome Browser, http://genome.ucsc.edu/ ; February 2009). B) FISH with BAC clones RP11-395A23 (AC010149) (chr2:231,304,236–231,476,367). The arrowhead indicates the deleted chromosome 2. D) Result of array-CGH analysis of chromosome 2 with Agilent Human Genome CGH microarray Kit G3 400 in patient 2. The 4.515 Mb interstitial deletion at bands q37.1q37.3 of chromosome 2 was comprised between oligomers A_16_P16076619 (232,963,736 bp) and A_16_P36124457(237,479,062 bp) flanked by oligomers A_16_P16076610 (232,954,321 bp) and A_16_P36124475 (237,483,914 bp). C) FISH with RP11-485M18 (AC079400)(chr2:236,766,818-236,919,215). The arrowhead shows the deleted chromosome 2.

    Journal: PLoS ONE

    Article Title: Genotype-Phenotype Correlation of 2q37 Deletions Including NPPC Gene Associated with Skeletal Malformations

    doi: 10.1371/journal.pone.0066048

    Figure Lengend Snippet: A) Result of array-CGH analysis of chromosome 2 with Agilent Human Genome CGH microarray Kit G3 400 in patient 1. The 1.914 Mb interstitial q37.1 deleted region of chromosome 2 extends between oligomers A_18_P13670199 (231,264,956 bp) and A_16_P00618306 (233,178,325 bp) flanked by oligomers A_16_P00615757 (231,257,468 bp) and A_16_P00618312 (233,181,399 bp) (UCSC Genome Browser, http://genome.ucsc.edu/ ; February 2009). B) FISH with BAC clones RP11-395A23 (AC010149) (chr2:231,304,236–231,476,367). The arrowhead indicates the deleted chromosome 2. D) Result of array-CGH analysis of chromosome 2 with Agilent Human Genome CGH microarray Kit G3 400 in patient 2. The 4.515 Mb interstitial deletion at bands q37.1q37.3 of chromosome 2 was comprised between oligomers A_16_P16076619 (232,963,736 bp) and A_16_P36124457(237,479,062 bp) flanked by oligomers A_16_P16076610 (232,954,321 bp) and A_16_P36124475 (237,483,914 bp). C) FISH with RP11-485M18 (AC079400)(chr2:236,766,818-236,919,215). The arrowhead shows the deleted chromosome 2.

    Article Snippet: Considering the phenotypic abnormalities of the patients, array CGH analysis (Agilent G3 400 K) was performed.

    Techniques: Microarray, Clone Assay