Whole genome uniparental isodisomy detected using single nucleotide polymorphism (SNP) microarray in molar pregnancy: a case report by Onyinye O. Okonkwo, Veronica Ortega, Sheila Kane, Galina Aldrete, Paulina Ramirez, Philip T. Valente, Gopalrao V.N. Velagaleti

“…High-resolution SNP microarray studies detected whole genome uniparental isodisomy. …”
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A hybrid of an automated multi-filter with a spatial bound particle swarm optimization for gene selection and cancer classification by Anas Arram, Masri Ayob, Musatafa Abbas Abbood Albadr, Dheeb Albashish, Alaa Sulaiman

“…Cancer is one of the most dangerous diseases and a leading cause of death globally. Therefore, early detection of cancer is critical for effective treatments. …”
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Identification of potential biomarkers and pathways related to major depressive disorder by integrated bioinformatic analysis and experimental validation by Ying Zeng, Lu-Qi Peng, Mei Zhang, Rong Zhong, Ke-Chao Nie, Wei Huang

“…Objective: To identify promising biomarkers for the pathogenesis of major depressive disorder (MDD). Methods: Microarray chips of MDD patients, including the GSE98793, GSE52790, and GSE39653 datasets, were obtained from the Gene Expression Omnibus database. …”
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Optimized T7 Amplification System for Microarray Analysis by C. Pabón, Z. Modrusan, M.V. Ruvolo, I.M. Coleman, S. Daniel, H. Yue, L.J. Arnold, M.A. Reynolds

“…Glass cDNA microarray technologies offer a highly parallel approach for profiling expressed gene sequences in disease-relevant tissues. …”
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Microarray analysis of the effects of Acthar Gel versus methylprednisolone in a model of focal segmental glomerulosclerosis in female rats by Kyle Hayes, Dale Wright

“…On Day 56, animals were sacrificed, and RNA samples of kidney cortex tissue were analyzed using microarrays. Compared with control, Acthar significantly decreased the expression of more genes related to inflammation, immune function, and fibrosis than MP. …”
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Genetic etiology and pregnancy outcomes of fetal hyperechoic kidneys: a retrospective analysis by Meiying Cai, Na Lin, Ziheng Xiao, Ziheng Xiao, Hailong Huang, Lin Zheng, Liangpu Xu

“…Chromosome karyotyping and chromosomal microarray analysis (CMA) were performed on fetuses displaying this phenotype on prenatal ultrasound. …”
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Analysis of a Series of 26 Cases With Prenatal Skeletal Dysplasia via Multiplatform Genetic Detection by Li‐min Cui, Hua‐ying Hu, Xiao‐mei Zhai, Ming‐fei Qi, Yan‐ming Liu, Cong‐ying Han, Jing Zhang, Ming Shen, Yu‐lan Xiang, Wen‐qi Chen, Kai Yang, Dong‐liang Zhang, Huan‐xia Xing

“…Materials and Methods In this study, we recruited 26 cases of SD and analyzed them with a designed sequential genetic detection. Chromosome karyotyping, microarray analysis (CMA), and whole exome sequencing (WES) techniques are performed as needed. …”
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P685: A single-center reevaluation and reanalysis of copy number variants of uncertain significance detected by chromosome microarray from consecutive pediatric patients by Wenjiao Li, Hongyan Chai, Autumn Diadamo, Yuan Dai, Peining Li, Michele Spencer-Manzon, Hui Zhang, Jiadi Wen

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Clinically relevant genetic variants of drug-metabolizing enzyme and transporter genes detected in Thai children and adolescents with autism spectrum disorder by Medhasi S, Pasomsub E, Vanwong N, Ngamsamut N, Puangpetch A, Chamnanphon M, Hongkaew Y, Limsila P, Pinthong D, Sukasem C

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A Sensitive and Fast microRNA Detection Platform Based on CRlSPR-Cas12a Coupled with Hybridization Chain Reaction and Photonic Crystal Microarray by Bingjie Xue, Bokang Qiao, Lixin Jia, Jimei Chi, Meng Su, Yanlin Song, Jie Du

“…The sensitive and fast detection of miRNAs is critical for diagnosis and prognosis. …”
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Application of chromosome microarray analysis and karyotyping in fetal cardiac abnormalities by Yun Guo, Xiaoqin Xin, Linju Zhou, Jungao Huang

“…Chromosome microarray analysis detected abnormalities in 6.58% (5/76) of the isolated cardiac abnormalities group and 27.27% (6/22) in the group with combined abnormalities, showing a significant statistical difference (P < 0.05). …”
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Computer Vision for Substrate Detection in High‐Throughput Biomaterial Screens Using Bright‐Field Microscopy by Robert Owen, Aishah Nasir, Mahetab H. Amer, Chenxue Nie, Xuan Xue, Laurence Burroughs, Chris Denning, Ricky D. Wildman, Faraz A. Khan, Morgan R. Alexander, Felicity R. A. J. Rose

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A universal DNA microarray for rapid fish species authentication by Patrizia Bade, Sebastian Stix, Kristina Kappel, Jan Fritsche, Ilka Haase, Andrew Torda, Nils Wax, Markus Fischer, Dirk Brandis, Ute Schröder

“…DNA microarrays are now used in fields such as gene expression analysis, pathogen/virus detection and identification of biomarkers. …”
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Cell-binding microarray application in diagnosis of hairy cell leukemia by A. N. Khvastunova, L. S. Al-Radi, N. M. Kapranov, O. S. Fedyanina, L. A. Gorgidze, S. A. Lugovskaya, E. V. Naumova, U. L. Dzhulakyan, A. V. Filatov, F. I. Ataullakhanov, S. A. Kuznetsova

“…We describe an application of a cell-binding microarray – to parallel study of morphology, tartrate-resistant acid phosphatase activity and detection of surface markers on peripheral blood lymphocytes of 90  atients with suspected hairy cell leukemia (HCL). …”
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Phenotype microarray-based assessment of metabolic variability in plant protoplasts by Alice Checcucci, Francesca Decorosi, Giulia Alfreducci, Roberto Natale, Agnese Bellabarba, Stefano Biricolti, Donatella Paffetti, Alessio Mengoni, Carlo Viti

“…Conclusions The standardized high-throughput system developed was effective for the metabolic characterization of plant protoplasts. …”
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Monitoring of Representational Difference Analysis Subtraction Procedures by Global Microarrays by T. Andersson, P. Unneberg, P. Nilsson, J. Odeberg, J. Quackenbush, J. Lundeberg

“…We demonstrate how global microarray technology can be used for the exploration of the differentially expressed genes extracted through representational difference analysis (RDA). …”
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Inflammatory Pathways in Parkinson’s Disease; A BNE Microarray Study by Pascal. F. Durrenberger, Edna Grünblatt, Francesca S. Fernando, Camelia Maria Monoranu, Jordan Evans, Peter Riederer, Richard Reynolds, David T. Dexter

“…The main focus of PD research is to better understand substantia nigra homeostasis disruption, particularly in relation to the wide-spread deposition of the aberrant protein α-synuclein. Microarray technology contributed towards PD research with several studies to date and one gene, ALDH1A1 (Aldehyde dehydrogenase 1 family, member A1), consistently reappeared across studies including the present study, highlighting dopamine (DA) metabolism dysfunction resulting in oxidative stress and most probably leading to neuronal cell death. …”
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Application of Chromosome Microarray in Diagnosis of Amniotic Fluid in Older Pregnant Women by Guangting Lu, Weiwu Liu, Chao Ou

“…Background: To improve the detection rate of chromosome abnormalities in fetuses and to reduce the birth defects rate in elderly pregnant women using chromosome karyotype analysis combined with the chromosome microarray analysis (CMA) technique. …”
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Implementation of NGS and SNP microarrays in routine forensic practice: opportunities and barriers by Sharlize Pedroza Matute, Sasitaran Iyavoo

“…NGS enables STR sequencing and SNP typing with enhanced discriminatory power, better performance with degraded DNA, and improved mixture deconvolution. Conversely, SNP microarrays offer a cost-effective solution for extended kinship testing, Forensic Investigative Genetic Genealogy (FIGG), and phenotypic prediction, though they are less effective with low-quality samples and DNA mixtures. …”
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Xq12q13.2 duplication detected in a child in selective exome screening by A. A. Dokshukina, Je. Shubina, D. N. Maslennikov, I. O. Sadelov, E. R. Tolmacheva, S. V. Ionushene, T. A. Bairova, L. V. Rychkova, D. Yu. Trofimov, D. N. Degtyarev

“…To describe the clinical and phenotypic features of a patient with a previously undescribed Xq12q13.2 duplication detected in the neonatal period.Materials and methods. …”
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