sequenom massarray platform (agena bioscience)
97
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agena bioscience
sequenom massarray platform
Sequenom Massarray Platform, supplied by agena bioscience, used in various techniques. Bioz Stars score: 97/100, based on 19543 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/massarray+analyzer+4+platform/MassARRAY+Nanodispenser+Samsung+LT/10__3390_slash_plants15203111-115-13-13
Average 97 stars, based on 19543 article reviews
Sequenom Massarray Platform, supplied by agena bioscience, used in various techniques. Bioz Stars score: 97/100, based on 19543 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/massarray+analyzer+4+platform/MassARRAY+Nanodispenser+Samsung+LT/10__3390_slash_plants15203111-115-13-13
Average 97 stars, based on 19543 article reviews
sequenom massarray platform - by Bioz Stars,
2026-11
97/100 stars
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Sequencing:Article Title: Characterization of Reference Materials for Genetic Testing of CYP2D6 Alleles Article Snippet: .. Five laboratories participated in this follow-up investigation using a variety of methods, including the matrix-assisted laser desorption/ionization-time of Next-Generation Sequencing:Article Title: Characterization of Reference Materials for Genetic Testing of CYP2D6 Alleles Article Snippet: .. Five laboratories participated in this follow-up investigation using a variety of methods, including the matrix-assisted laser desorption/ionization-time of Multiplex Assay:Article Title: Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi‐Ethnic Allele and Copy Number Variant Detection Article Snippet: .. The comprehensive pharmacogenetic panel uses multiplex polymerase chain reaction (PCR) and single base extension (SBE) using the Agena SpectroCHIP II and Article Title: Long-read HiFi sequencing of NUDT15: Phased full-gene haplotyping and pharmacogenomic allele discovery. Article Snippet: Saliva samples were collected using the Oragene Dx kit (OGD‐500; DNA Genotek) and DNA was isolated using the QiaSymphony (Qiagen). .. 2.2 | NUDT15 targeted genotyping Genotyping of three variant NUDT15 alleles [*2 (*3) (rs116855232), *4 (rs147390019), and *5 (rs186364861)] was performed using a comprehensive pharmacogenetic genotyping panel (S. A. Scott et al., 2020), which employs multiplex PCR and single base extension (SBE) using the Agena® SpectroCHIP® II and Article Title: Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi-Ethnic Allele and Copy Number Variant Detection. Article Snippet: .. The comprehensive pharmacogenetic panel uses multiplex polymerase chain reaction (PCR) and single base extension (SBE) using the Agena SpectroCHIP II and Polymerase Chain Reaction:Article Title: Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi‐Ethnic Allele and Copy Number Variant Detection Article Snippet: .. The comprehensive pharmacogenetic panel uses multiplex polymerase chain reaction (PCR) and single base extension (SBE) using the Agena SpectroCHIP II and Article Title: Long-read HiFi sequencing of NUDT15: Phased full-gene haplotyping and pharmacogenomic allele discovery. Article Snippet: Saliva samples were collected using the Oragene Dx kit (OGD‐500; DNA Genotek) and DNA was isolated using the QiaSymphony (Qiagen). .. 2.2 | NUDT15 targeted genotyping Genotyping of three variant NUDT15 alleles [*2 (*3) (rs116855232), *4 (rs147390019), and *5 (rs186364861)] was performed using a comprehensive pharmacogenetic genotyping panel (S. A. Scott et al., 2020), which employs multiplex PCR and single base extension (SBE) using the Agena® SpectroCHIP® II and Article Title: Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi-Ethnic Allele and Copy Number Variant Detection. Article Snippet: .. The comprehensive pharmacogenetic panel uses multiplex polymerase chain reaction (PCR) and single base extension (SBE) using the Agena SpectroCHIP II and Software:Article Title: Characterization of Reference Materials for TPMT and NUDT15: A GeT-RM Collaborative Project. Article Snippet: From the Department of Medical and Molecular Genetics,* Indiana University School of Medicine, Indianapolis, Indiana; the Division of Clinical Pharmacology, Toxicology, and Therapeutic Innovation,y Children’s Mercy Kansas City, Kansas City, Missouri; RPRD Diagnostics,z Milwaukee, Wisconsin; the Department of Pediatrics,x Section on Genomic Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin; Sema4,{ Stamford, Connecticut; the Department of Genetics and Genomic Sciences,k Icahn School of Medicine at Mount Sinai, New York, New York; the Department of Pediatrics,** University of MissourieKansas City School of Medicine, Kansas City, Missouri; the Department of Laboratory Medicine and Pathology,yy Mayo Clinic, Rochester, Minnesota; the Coriell Institute for Medical Research,zz Camden, New Jersey; the Department of Pathology,xx Stanford University, Stanford, California; the Clinical Genomics Laboratory,{{ Stanford Healthcare, Palo Alto, California; the Department of Pathology, Immunology, and Laboratory Medicine,kk University of Florida College of Medicine, Gainesville, Florida; and the Division of Laboratory Systems,*** Centers for Disease Control and Prevention, Atlanta, Georgia Mass Spectrometry:Article Title: The relationship between polymorphism rs12449964 of the phosphatidylethanolamine- N-methyltransferase gene and hypertriglyceridemia and obesity in patients with type 2 diabetes Article Snippet: .. Genotyping of PEMT gene polymorphism (C>T, rs12449964) was performed by laser desorption / ionization time-of-flight mass spectrometry using the Variant Assay:Article Title: Long-read HiFi sequencing of NUDT15: Phased full-gene haplotyping and pharmacogenomic allele discovery. Article Snippet: Saliva samples were collected using the Oragene Dx kit (OGD‐500; DNA Genotek) and DNA was isolated using the QiaSymphony (Qiagen). .. 2.2 | NUDT15 targeted genotyping Genotyping of three variant NUDT15 alleles [*2 (*3) (rs116855232), *4 (rs147390019), and *5 (rs186364861)] was performed using a comprehensive pharmacogenetic genotyping panel (S. A. Scott et al., 2020), which employs multiplex PCR and single base extension (SBE) using the Agena® SpectroCHIP® II and Genotyping:Article Title: NOX Subunit Gene Polymorphisms and the Risk of Chronic Artery Disease in Type 2 Diabetes Patients Article Snippet: 0027 NOX Subunit Gene Polymorphisms and the Risk of Chronic Artery Disease in Type 2 Diabetes Patients Iuliia Azarova, Ekaterina Shkurat, Elena Klyosova, Alexey Polonikov Kursk State Medical University Abstract Background: Oxidative stress is a key feature of type 2 diabetes (T2D) and coronary artery disease (CAD).. NADPH oxidase (NOX) is the main producer of reactive oxygen species and therefore genes encoding NOX subunits may contribute to the disease susceptibility.. The present study investigated whether polymorphisms of genes encoding cytochrome a (CYBA), Rac family small GTPase 1 (RAC1) and neutrophil cytosolic factor 4 (NCF4) jointly contribute to the risk for CAD in T2D patients of Central Russia. |