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massarray-system-1  (agena bioscience)


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    Structured Review

    agena bioscience massarray-system-1
    Massarray System 1, supplied by agena bioscience, used in various techniques. Bioz Stars score: 96/100, based on 19165 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/massarray+genotyping+data/massarray-system-1/custom%40massarray-system-1%4034008880
    Average 96 stars, based on 19165 article reviews
    massarray-system-1 - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Methylation:

    Article Title: Analysis of MIR155HG gene polymorphisms and ulcerative colitis susceptibility in the Chinese Han Population
    Article Snippet: udy included 84 UC patients and 216 matched healthy controls. Four single nucleotide polymorphisms (SNPs) of MIR155HG (rs1893650, rs2282471, rs2829803, and rs2829806) were genotyped using the Sequenom MassARRAY platform. Function prediction of SNPs were conducted using RNAfold databases. We observed MIR155HG rs2282471 polymorphism was significantly associated with a reduced risk of UC. Specifically

    Software:

    Article Title: Analysis of MIR155HG gene polymorphisms and ulcerative colitis susceptibility in the Chinese Han Population
    Article Snippet: udy included 84 UC patients and 216 matched healthy controls. Four single nucleotide polymorphisms (SNPs) of MIR155HG (rs1893650, rs2282471, rs2829803, and rs2829806) were genotyped using the Sequenom MassARRAY platform. Function prediction of SNPs were conducted using RNAfold databases. We observed MIR155HG rs2282471 polymorphism was significantly associated with a reduced risk of UC. Specifically

    Luciferase:

    Article Title: Analysis of MIR155HG gene polymorphisms and ulcerative colitis susceptibility in the Chinese Han Population
    Article Snippet: udy included 84 UC patients and 216 matched healthy controls. Four single nucleotide polymorphisms (SNPs) of MIR155HG (rs1893650, rs2282471, rs2829803, and rs2829806) were genotyped using the Sequenom MassARRAY platform. Function prediction of SNPs were conducted using RNAfold databases. We observed MIR155HG rs2282471 polymorphism was significantly associated with a reduced risk of UC. Specifically

    DNA Methylation Assay:

    Article Title: Analysis of MIR155HG gene polymorphisms and ulcerative colitis susceptibility in the Chinese Han Population
    Article Snippet: udy included 84 UC patients and 216 matched healthy controls. Four single nucleotide polymorphisms (SNPs) of MIR155HG (rs1893650, rs2282471, rs2829803, and rs2829806) were genotyped using the Sequenom MassARRAY platform. Function prediction of SNPs were conducted using RNAfold databases. We observed MIR155HG rs2282471 polymorphism was significantly associated with a reduced risk of UC. Specifically

    Mass Spectrometry:

    Article Title: Analysis of MIR155HG gene polymorphisms and ulcerative colitis susceptibility in the Chinese Han Population
    Article Snippet: udy included 84 UC patients and 216 matched healthy controls. Four single nucleotide polymorphisms (SNPs) of MIR155HG (rs1893650, rs2282471, rs2829803, and rs2829806) were genotyped using the Sequenom MassARRAY platform. Function prediction of SNPs were conducted using RNAfold databases. We observed MIR155HG rs2282471 polymorphism was significantly associated with a reduced risk of UC. Specifically



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    Image Search Results


    This figure shows the 4 steps of the SNPflow data analysis wizard. In brief, the first step allows the uploading of either SDS files (ABI 7900HT) or TyperAnalyzer 4.0 (MassARRAY) files. For TyperAnalyzer files, a second input field asks for the name of the result group under which results shall be grouped. The second step checks the validity of the IDs found in the uploaded and reports IDs, which are not found in the study definition and shall thus be deleted. Step 3 converts the found genotype designations to standard genotypes and allows entering the name of the result, the operator name, an optional comment and the rs-number of the SNP in HapMap and the 1000 Genomes Project. This is useful in case that a SNP ID changed between the current dbSNP release and the dbSNP release used in HapMap, as happened for some SNPs. For convenience, the result name is automatically pre-set as HapMap lookup. In multiplex assays, pagination allows navigating through the single SNPs. For quality reasons a manual confirmation of each conversion is required (Checkbox “All settings are correct”). Finally, step 4 confirms the successful analysis and brings the user to the report. Exemplary abbreviation used in this figure: NTC, Non-template control; ER, annulled samples (“error”), i.e. DNA samples present on the plates, but known to be flawed. The IDs of these samples were thus replaced with “ER” in order to avoid data collection for these samples.

    Journal: PLoS ONE

    Article Title: SNPflow: A Lightweight Application for the Processing, Storing and Automatic Quality Checking of Genotyping Assays

    doi: 10.1371/journal.pone.0059508

    Figure Lengend Snippet: This figure shows the 4 steps of the SNPflow data analysis wizard. In brief, the first step allows the uploading of either SDS files (ABI 7900HT) or TyperAnalyzer 4.0 (MassARRAY) files. For TyperAnalyzer files, a second input field asks for the name of the result group under which results shall be grouped. The second step checks the validity of the IDs found in the uploaded and reports IDs, which are not found in the study definition and shall thus be deleted. Step 3 converts the found genotype designations to standard genotypes and allows entering the name of the result, the operator name, an optional comment and the rs-number of the SNP in HapMap and the 1000 Genomes Project. This is useful in case that a SNP ID changed between the current dbSNP release and the dbSNP release used in HapMap, as happened for some SNPs. For convenience, the result name is automatically pre-set as HapMap lookup. In multiplex assays, pagination allows navigating through the single SNPs. For quality reasons a manual confirmation of each conversion is required (Checkbox “All settings are correct”). Finally, step 4 confirms the successful analysis and brings the user to the report. Exemplary abbreviation used in this figure: NTC, Non-template control; ER, annulled samples (“error”), i.e. DNA samples present on the plates, but known to be flawed. The IDs of these samples were thus replaced with “ER” in order to avoid data collection for these samples.

    Article Snippet: SNPflow is a lightweight, intuitive and easily deployable application, which processes genotype data from Sequenom MassARRAY (iPLEX) and ABI 7900HT (TaqMan, KASPar) systems and is extendible to other genotyping methods as well.

    Techniques: Multiplex Assay

    Validation of 42 SNPs at the RDV2 locus

    Journal: BMC Plant Biology

    Article Title: Genetic identification of SNP markers linked to a new grape phylloxera resistant locus in Vitis cinerea for marker-assisted selection

    doi: 10.1186/s12870-018-1590-0

    Figure Lengend Snippet: Validation of 42 SNPs at the RDV2 locus

    Article Snippet: A comparison of the genotype data from Sequenom MassARRAY and the TASSEL SNP calling pipeline was performed to validate SNPs.

    Techniques:

    Genotyping errors detected in F 1 individuals after Sequenom  MassARRAY  genotyping

    Journal: BMC Plant Biology

    Article Title: Genetic identification of SNP markers linked to a new grape phylloxera resistant locus in Vitis cinerea for marker-assisted selection

    doi: 10.1186/s12870-018-1590-0

    Figure Lengend Snippet: Genotyping errors detected in F 1 individuals after Sequenom MassARRAY genotyping

    Article Snippet: A comparison of the genotype data from Sequenom MassARRAY and the TASSEL SNP calling pipeline was performed to validate SNPs.

    Techniques:

    Table 1.

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: Population, genetic, and antigenic diversity of the apicomplexan Eimeria tenella and their relevance to vaccine development

    doi: 10.1073/pnas.1506468112

    Figure Lengend Snippet: Table 1.

    Article Snippet: Returning to the Sequenom MassARRAY genotyping data, we found 46% of all samples submitted for typing to be polyclonal as determined by a multiple SNP identity at one or more loci.

    Techniques: Genome Wide