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Sequenom massarray assay design suite software
Massarray Assay Design Suite Software, supplied by Sequenom, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/massarray+design+suite/assay+design+massarray+software/pm41076047-61-7-12
Average 86 stars, based on 1 article reviews
massarray assay design suite software - by Bioz Stars, 2026-10
86/100 stars

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Article Title: Correlation of MicroRNA 17-92 Cluster Host Gene (MIR17HG) Polymorphisms With Susceptibility and Prognosis for Multiple Myeloma.
Article Snippet: Polymorphisms of MIR17HG rs7336610 and rs4284505 were closely associated with multiple myeloma (MM) risk, severity, and prognosis.. Further, haplotypes AC and GC (rs4284505-rs1428) were significantly linked to MM risk, as was haplotype CA (rs7336610-rs4284505).. Purpose: To explore the correlation of MIR17HG polymorphism with susceptibility and prognosis of multiple myeloma (MM).

Article Title: An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders.
Article Snippet: a Instituto de Investigación Sanitaria (IDIS) de Santiago de Compostela, Servizo Galego de Saúde (SERGAS), Santiago de Compostela, Spain b Fundación Pública Galega de Medicina Xenómica, Santiago de Compostela, Spain c Servizo de Psiquiatría, Complexo Hospitalario Universitario de Santiago de Compostela, Servizo Galego de Saúde (SERGAS), Santiago de Compostela, Spain d Grupo de Medicina Xenómica, Universidade de Santiago de Compostela, Santiago de Compostela, Spain

Article Title: Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's disease
Article Snippet: Assays for all SNPs were designed using the eXTEND suite and MassARRAY Assay Design software version 3.1 (Sequenom Inc.).

Article Title: Genetic association analysis of miRNA SNPs implicates MIR145 in breast cancer susceptibility.
Article Snippet: Using the MassARRAY® Assay Design Suite v1.0 software (SEQUENOM Inc., San Diego, CA, USA) we were able to create a single multiplex PCR genotyping assay containing 24 miR-SNPs from our preliminary selection (See Table 2).

Article Title: Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy
Article Snippet: Genotyping assays were designed using Sequenom MassARRAY Assay ® Design Suite, version 1.0 (Sequenom Inc.).

Software:

Article Title: Th2 cell regulatory and effector molecules single nucleotide polymorphisms and periodontitis
Article Snippet: 1Faculty of Dentistry, The University of Hong Kong, Hong Kong SAR, China 2RytimeDental Hospital, Chengdu, Sichuan, China 3School of Biomedical Sciences, Li Ka Shing Faculty ofMedicine, The University of Hong Kong, Hong Kong SAR, China 4Thornleigh Periodontal Clinic, Thornleigh, New SouthWales, Australia 5Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty ofMedicine, The University of Hong Kong, Hong Kong SAR, China 6Current address: Phil Rivers Technology, NanshanDistrict, Haitian Second Road, Shenzhen, China Correspondence W.K.. Leung, FacultyofDentistry, TheUniversity ofHongKong, PrincePhilipDentalHospital, Room3B44, 34HospitalRoad, SaiYingPun, HongKongSAR,China E-mail: ewkleung@hku.hk Abstract Aim: To investigate the association between T helper 2 (Th2) cell regulatory and effector molecules’ genetic polymorphisms and periodontitis.

Article Title: The association of ARR3 genetic polymorphisms with pathologic myopia in Northern Chinese population.
Article Snippet: Purpose: The study is conducted to illustrate the relationship between the single nucleotide polymorphisms (SNPs) of ARR3 and pathologic myopia (PM) among the general public residing in Northern China.. Methods: PM patients and the emmetropic controls were recruited in Northern China.. The venous blood samples of subjects were collected, following which DNA were extracted.

Article Title: Association of a COL1A1 Gene Haplotype with Pathologic Myopia in a Northern Chinese Han Population.
Article Snippet: 14 To investigate the relationship between COL1A1 variations and the susceptibility to pathologic 15 myopia (PM) among the general population in Northern China, we included 525 PM patients and 16 1105 non-myopic controls.. All PM patients underwent comprehensive ophthalmologic 17 examinations.. DNA was extracted from peripheral venous blood samples and genotyped using the 18 MassArray System.

Polymerase Chain Reaction:

Article Title: Th2 cell regulatory and effector molecules single nucleotide polymorphisms and periodontitis
Article Snippet: 1Faculty of Dentistry, The University of Hong Kong, Hong Kong SAR, China 2RytimeDental Hospital, Chengdu, Sichuan, China 3School of Biomedical Sciences, Li Ka Shing Faculty ofMedicine, The University of Hong Kong, Hong Kong SAR, China 4Thornleigh Periodontal Clinic, Thornleigh, New SouthWales, Australia 5Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty ofMedicine, The University of Hong Kong, Hong Kong SAR, China 6Current address: Phil Rivers Technology, NanshanDistrict, Haitian Second Road, Shenzhen, China Correspondence W.K.. Leung, FacultyofDentistry, TheUniversity ofHongKong, PrincePhilipDentalHospital, Room3B44, 34HospitalRoad, SaiYingPun, HongKongSAR,China E-mail: ewkleung@hku.hk Abstract Aim: To investigate the association between T helper 2 (Th2) cell regulatory and effector molecules’ genetic polymorphisms and periodontitis.

Genotyping Assay:

Article Title: The association of ARR3 genetic polymorphisms with pathologic myopia in Northern Chinese population.
Article Snippet: Purpose: The study is conducted to illustrate the relationship between the single nucleotide polymorphisms (SNPs) of ARR3 and pathologic myopia (PM) among the general public residing in Northern China.. Methods: PM patients and the emmetropic controls were recruited in Northern China.. The venous blood samples of subjects were collected, following which DNA were extracted.



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sP and sN calculation

Journal: The Malaysian Journal of Medical Sciences : MJMS

Article Title: Development of DNA-Based Lateral Flow Assay for Detection of LDLR Gene Mutation for Familial Hypercholesterolemia

doi: 10.21315/mjms2024.31.3.6

Figure Lengend Snippet: sP and sN calculation

Article Snippet: Briefly, a panel assay was designed involving the primer design for the PCR process and the iPLEX reaction for the variant of interest (E101K) using the MassARRAY ® Assay Design Suite (ADS) software (Agena Bioscience, USA).

Techniques:

MassARRAY ® spectrum analysis for gBlock gene fragment and representative clinical samples for E101K, LDLR gene. A) Wild-type gBlock: negative. B) Mutant gBlock: positive. C) Healthy control, HC 1: negative. D) FH 1: positive. The presence of one peak (red boxes) on the spectrum analysis indicates homozygous form, while the presence of two peaks (red boxes) on the spectrum analysis indicates heterozygous form

Journal: The Malaysian Journal of Medical Sciences : MJMS

Article Title: Development of DNA-Based Lateral Flow Assay for Detection of LDLR Gene Mutation for Familial Hypercholesterolemia

doi: 10.21315/mjms2024.31.3.6

Figure Lengend Snippet: MassARRAY ® spectrum analysis for gBlock gene fragment and representative clinical samples for E101K, LDLR gene. A) Wild-type gBlock: negative. B) Mutant gBlock: positive. C) Healthy control, HC 1: negative. D) FH 1: positive. The presence of one peak (red boxes) on the spectrum analysis indicates homozygous form, while the presence of two peaks (red boxes) on the spectrum analysis indicates heterozygous form

Article Snippet: Briefly, a panel assay was designed involving the primer design for the PCR process and the iPLEX reaction for the variant of interest (E101K) using the MassARRAY ® Assay Design Suite (ADS) software (Agena Bioscience, USA).

Techniques: Mutagenesis, Control