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sureprint g3 human cgh microarray kit, 2 × 400k chip  (Agilent technologies)


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    Agilent technologies sureprint g3 human cgh microarray kit, 2 × 400k chip
    Sureprint G3 Human Cgh Microarray Kit, 2 × 400k Chip, 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/400k+sureprint+g3+cgh+microarray/pm35088582-393-9-11
    Average 90 stars, based on 1 article reviews
    sureprint g3 human cgh microarray kit, 2 × 400k chip - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Hybridization:

    Article Title: Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia
    Article Snippet: .. Routine genetic testing was performed whenever clinically relevant, including copy-number variation (CNV) analysis by high-resolution array-based comparative genomic hybridization (aCGH) using (1) 180k CytoSure ISCA v2 array (Oxford Gene Technology; individuals 10A–D), (2) 180k SurePrint G3 CGH microarray as described 10 (Agilent; individual 11), or (3) 400k SurePrint G3 CGH microarray, as described 11 (Agilent, individuals 12 and 13). .. Affected individuals with a negative aCGH result underwent whole-exome sequencing (WES) on an Illumina HiSeq platform according to the following paradigms: (1) trio-based clinical diagnostic WES (individuals 1, 2, 6, 7, and 9), (2) trio-based WES in a research laboratory (individuals 3 and 4), or (3) WES of an affected individual followed by single site testing in parental DNA samples (individuals 5 and 8; see Table S1 for further details).

    Microarray:

    Article Title: Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia
    Article Snippet: .. Routine genetic testing was performed whenever clinically relevant, including copy-number variation (CNV) analysis by high-resolution array-based comparative genomic hybridization (aCGH) using (1) 180k CytoSure ISCA v2 array (Oxford Gene Technology; individuals 10A–D), (2) 180k SurePrint G3 CGH microarray as described 10 (Agilent; individual 11), or (3) 400k SurePrint G3 CGH microarray, as described 11 (Agilent, individuals 12 and 13). .. Affected individuals with a negative aCGH result underwent whole-exome sequencing (WES) on an Illumina HiSeq platform according to the following paradigms: (1) trio-based clinical diagnostic WES (individuals 1, 2, 6, 7, and 9), (2) trio-based WES in a research laboratory (individuals 3 and 4), or (3) WES of an affected individual followed by single site testing in parental DNA samples (individuals 5 and 8; see Table S1 for further details).



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    Features and experimental details of CNV detection platforms used in this study
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    Features and experimental details of CNV detection platforms used in this study

    Journal: BMC Genomics

    Article Title: Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans

    doi: 10.1186/s12864-017-3658-x

    Figure Lengend Snippet: Features and experimental details of CNV detection platforms used in this study

    Article Snippet: Agilent SurePrint G3 Human CGH Microarray, 2×400K (Design ID 021850) , 411,056 (60mers) , 5.3 kb overall median probe spacing (4.6 kb in Refseq genes) , Service Provider , Agilent Genomics Workbench 7.0 , 58,61 , 50,48.

    Techniques: Software, Genome Wide, Microarray