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180k oligonucleotides array cgh analysis  (Agilent technologies)


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    Agilent technologies 180k oligonucleotides array cgh analysis
    180k Oligonucleotides Array Cgh Analysis, 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/array+cgh+analysis/pm38185782-5333-5-6
    Average 90 stars, based on 1 article reviews
    180k oligonucleotides array cgh analysis - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Abstracts from the 56 th European Society of Human Genetics (ESHG) Conference: e-Posters.
    Article Snippet: Genetic investigation was performed using 180K Agilent oligonucleotides array CGH analysis according to the manufacturer’s instructions.

    Article Title: KDM1A genotyping and expression in 146 sporadic somatotroph pituitary adenomas.
    Article Snippet: Importance: A paradoxical increase of growth hormone (GH) following oral glucose load has been described in ∼30% of patients with acromegaly and has been related to the ectopic expression of the glucose-dependent insulinotropic polypeptide (GIP) receptor (GIPR) in somatotropinomas.. Recently, we identified germline pathogenic variants and somatic loss of heterozygosity of lysine demethylase 1A (KDM1A) in patients with GIP-dependent primary bilateral macronodular adrenal hyperplasia with Cushing's syndrome.. The ectopic expression of GIPR in both adrenal and pituitary lesions suggests a common molecular mechanism.

    Article Title: Clinical and molecular cytogenetic studies of five new patients with 20q11q12 deletion and review of the literature: Proposition of two critical regions.
    Article Snippet: It was conducted using oligo 60k Agilent® array for Patients #1, #2, and #3, and oligo 180k Agilent® array (Agilent technologies, Santa, Clara, CA, USA) for Patient #5.

    Microarray:

    Article Title: Phenotypic spectrum in Weiss-Kruszka syndrome caused by ZNF462 variants: Three new patients and literature review.
    Article Snippet: .. Array-CGH microarray utilized peripheral blood and 180k microarray slides from Agilent Technologies, following the manufacturer’s guidelines. .. Scanned images underwent processing through Agilent Genomic Workbench version 6.5 and Cartagenia software (Agilent Technologies).

    Article Title: Amplification of Mutant NRAS in Melanocytic Tumors With Features of Spitz Tumors.
    Article Snippet: .. For 5 cases, copy number variation was evaluated by array comparative genomic hybridization (CGH) on Agilent SurePrint G3 Human CGH Microarray 4 180K arrays with commercially available normal reference DNA. ..

    Article Title: DNA sequence and chromatin differentiate sequence-specific transcription factor binding in the human malaria parasite Plasmodium falciparum.
    Article Snippet: .. Overall, the total number of dsDNA probes was 174 550 spots, which were arrayed using an Agilent Technologies 4 × 180k microarray design. .. Overall, the total number of dsDNA probes was 174 550 spots, which were arrayed using an Agilent Technologies 4 × 180k microarray design.

    Article Title: DNA sequence and chromatin differentiate sequence-specific transcription factor binding in the human malaria parasite Plasmodium falciparum.
    Article Snippet: .. Additionally, each DNA probe was replicated in random areas of the microarray surface (four C AC AC A / GTGC AC replicates and three GT AC / TGCA TGCA replicates per orientation), which brought the total number of DNA probes to 174,550 spots for a 4 × 180k microarray (Agilent Technologies). ..

    Article Title: Novel PUF60 variant suggesting an interaction between Verheij and Cornelia de Lange syndrome: phenotype description and review of the literature
    Article Snippet: .. Array-CGH microarray involved the use of peripheral blood and 180k microarray slides from Agilent Technologies (Santa Clara, CA), following the manufacturer’s protocols. .. Scanned images were processed using Agilent Genomic Workbench version 6.5 and Cartagenia software (Agilent Technologies).

    Hybridization:

    Article Title: Amplification of Mutant NRAS in Melanocytic Tumors With Features of Spitz Tumors.
    Article Snippet: .. For 5 cases, copy number variation was evaluated by array comparative genomic hybridization (CGH) on Agilent SurePrint G3 Human CGH Microarray 4 180K arrays with commercially available normal reference DNA. ..



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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