cytosure® oligo array isca v2 4 × 180 k platform (Oxford Gene Technology)
90
Structured Review
Oxford Gene Technology
cytosure® oligo array isca v2 4 × 180 k platform
Cytosure® Oligo Array Isca V2 4 × 180 K Platform, supplied by Oxford Gene Technology, 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/isca+array/180k+feature+whole+genome+microarray+cytosure+iscav2/pm39858586-102-16-17
Average 90 stars, based on 1 article reviews
Cytosure® Oligo Array Isca V2 4 × 180 K Platform, supplied by Oxford Gene Technology, 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/isca+array/180k+feature+whole+genome+microarray+cytosure+iscav2/pm39858586-102-16-17
Average 90 stars, based on 1 article reviews
cytosure® oligo array isca v2 4 × 180 k platform - by Bioz Stars,
2026-09
90/100 stars
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Hybridization:Article Title: Exon 21 deletion in the OPHN1 gene in a family with syndromic X-linked intellectual disability Article Snippet: The arrayCGH analysis by using Article Title: Typical Clinical Presentation of an Autosomal Dominant Polycystic Kidney Disease Patient with an Atypical Genetic Pattern Article Snippet: This test was carried out using the CytoSure ® Oligo array ISCA v2 4 × 180 k Article Title: Typical Clinical Presentation of an Autosomal Dominant Polycystic Kidney Disease Patient with an Atypical Genetic Pattern. Article Snippet: This test was carried out using the CytoSure® Oligo array ISCA v2 4 × 180 k Article Title: CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms Article Snippet: Comparative genomic hybridization (CGH) assays were conducted at the CHUSJ using a 135k-feature whole-genome microarray (SignatureChip OS2.0 manufactured for Signature Genomic Laboratories (Spokane, WA, USA) by Roche NimbleGen, Madison, WI, USA; based on UCSC 2006 hg18 assembly), or at the CHUS using a Microarray:Article Title: Exon 21 deletion in the OPHN1 gene in a family with syndromic X-linked intellectual disability Article Snippet: The arrayCGH analysis by using Article Title: Typical Clinical Presentation of an Autosomal Dominant Polycystic Kidney Disease Patient with an Atypical Genetic Pattern Article Snippet: This test was carried out using the CytoSure ® Oligo array ISCA v2 4 × 180 k Article Title: Typical Clinical Presentation of an Autosomal Dominant Polycystic Kidney Disease Patient with an Atypical Genetic Pattern. Article Snippet: This test was carried out using the CytoSure® Oligo array ISCA v2 4 × 180 k Article Title: CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms Article Snippet: Comparative genomic hybridization (CGH) assays were conducted at the CHUSJ using a 135k-feature whole-genome microarray (SignatureChip OS2.0 manufactured for Signature Genomic Laboratories (Spokane, WA, USA) by Roche NimbleGen, Madison, WI, USA; based on UCSC 2006 hg18 assembly), or at the CHUS using a |