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Oxford Gene Technology 180k custom oligonucleotide microarray
Copy number status and fragment orientation as revealed by chromosomal <t> microarray </t> (CMA) and whole genome sequencing (WGS) of the complex rearrangements.
180k Custom Oligonucleotide Microarray, 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/180k+oligonucleotide+microarray/60k+cytosure+constitutional+v3+microarray/pmc06258378-313-22-38
Average 90 stars, based on 1 article reviews
180k custom oligonucleotide microarray - by Bioz Stars, 2026-10
90/100 stars

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1) Product Images from "Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization"

Article Title: Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization

Journal: PLoS Genetics

doi: 10.1371/journal.pgen.1007780

Copy number status and fragment orientation as revealed by chromosomal  microarray  (CMA) and whole genome sequencing (WGS) of the complex rearrangements.
Figure Legend Snippet: Copy number status and fragment orientation as revealed by chromosomal microarray (CMA) and whole genome sequencing (WGS) of the complex rearrangements.

Techniques Used: Microarray, Sequencing

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Hybridization:

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Article Snippet: .. Whole-Genome Array-Based Comparative Genomic Assay (a-CGH) A high-resolution whole-genome array-based comparative genomic hybridization (a-CGH) analysis was performed on the genomic DNA of the patient and their relatives, using the Cytosure Oligo array ISCA 4x180K OGT (Oxford Gene Technology, Oxford, UK), resolution ~50–60 Kb. ..

Article Title: Single-cell dissection of cervix and placenta reveal both novel and overlapping cell types
Article Snippet: DNA quality and concentration were assessed by NanoDrop ND-1000 Spectrophotometer (Thermo Fisher Scientific) and Qubit 2.0 Fluorometer (Invitrogen). .. Analysis of the copy number profile was then carried out by array comparative genomic hybridization (aCGH) using the 8×60 K CytoSure ISCA v3 microarray (Oxford Gene Technology). .. Results were analyzed using the CytoSure Interpret software (Oxford Gene Technology).

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Article Snippet: Peripheral blood genomic DNA (gDNA) was isolated using the PureLinkTM Genomic DNA Mini Kit (ThermoFisher Scientfic, Waltham, MA) according to the manufacturer’s protocol. .. Array-based comparative genomic hybridization (array-CGH) was performed using the CytoSure Constitutional Kit, version 3, 4 × 180k (Oxford Gene Technology) by following the manufacturer’s recommendations. .. NGS with an Epilepsy Panel comprising 308 genes was then performed for the proband in a private laboratory (Invitae Corporation, San Francisco, CA), as previously described [ ].

Article Title: Identification and characterization of stromal-like cells with CD207 +/low CD1a +/low phenotype derived from histiocytic lesions - a perspective in vitro model for drug testing.
Article Snippet: Array comparative genomic hybridization (aCGH) DNA from sl-pHCs cell lines was extracted using the Sherlock AX DNA isolation kit (A&A Biotechnology, Gdansk, Poland), according to the manufacturer’s instructions. .. Array comparative genomic hybridization (aCGH) was performed using the 60K CytoSure Constitutional v3 microarray (Oxford Gene Technology, Oxford, UK), according to the manufacturer’s protocol. .. Quality control measures were monitored using CytoSure Interpret Software (Oxford Gene Technology).

Microarray:

Article Title: Single-cell dissection of cervix and placenta reveal both novel and overlapping cell types
Article Snippet: DNA quality and concentration were assessed by NanoDrop ND-1000 Spectrophotometer (Thermo Fisher Scientific) and Qubit 2.0 Fluorometer (Invitrogen). .. Analysis of the copy number profile was then carried out by array comparative genomic hybridization (aCGH) using the 8×60 K CytoSure ISCA v3 microarray (Oxford Gene Technology). .. Results were analyzed using the CytoSure Interpret software (Oxford Gene Technology).

Article Title: Hysteroscopic resection as primary management in case of early pregnancy loss: time for a paradigm shift?
Article Snippet: Research question: What is the potential role of hysteroscopic resection (HsR) of early pregnancy loss (EPL) according to its feasibility and efficacy, including in the outpatient setting, for early-stage pregnancies?. Design: Retrospective cohort study and literature review.. Patients undergoing HsR of EPL in the authors’ tertiary fertility centre between November 2022 and January 2024 were included.

Article Title: Identification and characterization of stromal-like cells with CD207 +/low CD1a +/low phenotype derived from histiocytic lesions - a perspective in vitro model for drug testing.
Article Snippet: Array comparative genomic hybridization (aCGH) DNA from sl-pHCs cell lines was extracted using the Sherlock AX DNA isolation kit (A&A Biotechnology, Gdansk, Poland), according to the manufacturer’s instructions. .. Array comparative genomic hybridization (aCGH) was performed using the 60K CytoSure Constitutional v3 microarray (Oxford Gene Technology, Oxford, UK), according to the manufacturer’s protocol. .. Quality control measures were monitored using CytoSure Interpret Software (Oxford Gene Technology).

other:

Article Title: Expanding the phenotype of copy number variations involving NR0B1 (DAX1).
Article Snippet: 46,XY gonadal dysgenesis (GD) is a disorder of sex development due to incomplete gonadal differentiation into testes, resulting in female to ambiguous external genitalia.. Duplications at the Xp21.2 locus involving the NR0B1 (DAX1) gene have previously been associated with 46,XY GD.. More recently, a complex structural variant not directly involving NR0B1 has been reported in 46,XY GD illustrating that the mechanism of how copy number variants (CNVs) at Xp21.2 may cause 46,XY gonadal dysgenesis is not yet fully understood.

Article Title: Two novel compound heterozygous HOXB1 variants in congenital facial palsy: A case report and a brief review of the literature.
Article Snippet: Struttura Complessa di Neuropsichiatria Infantile, Dipartimento Materno-Infantile, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy R&I Genetics, Padova, Italy Struttura Complessa di Genetica Medica, Dipartimento Materno-Infantile, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy Struttura Semplice Dipartimentale di Neuroradiologia, Dipartimento di Diagnostica per Immagini e Medicina di Laboratorio, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy

Article Title: Typical Clinical Presentation of an Autosomal Dominant Polycystic Kidney Disease Patient with an Atypical Genetic Pattern.
Article Snippet: The CGH array produced a negative outcome, consistent with the technique’s detection threshold for mosaicism at 20%. his test was carried out using the CytoSu e® Oligo array ISCA v2 4×180k platform (Oxford Gene Tech ology, Oxford, UK), with an average resolution of 80 Kb.



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Copy number status and fragment orientation as revealed by chromosomal <t> microarray </t> (CMA) and whole genome sequencing (WGS) of the complex rearrangements.
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Image Search Results


Copy number status and fragment orientation as revealed by chromosomal  microarray  (CMA) and whole genome sequencing (WGS) of the complex rearrangements.

Journal: PLoS Genetics

Article Title: Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization

doi: 10.1371/journal.pgen.1007780

Figure Lengend Snippet: Copy number status and fragment orientation as revealed by chromosomal microarray (CMA) and whole genome sequencing (WGS) of the complex rearrangements.

Article Snippet: In 13 cases (P2046_133, P2109_123, P2109_150, P2109_151, P2109_162, P2109_188, P2109_190, P2109_302, P4855_511, P4855_512, P2109_176, P1426_301, P2109_185), the CMA was performed with an 180K custom oligonucleotide microarray with whole genome coverage and a median resolution of approximately 18 kb (Oxford Gene Technology (OGT), Oxfordshire, UK).

Techniques: Microarray, Sequencing