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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+iplextm+gold/massarray-system-1/custom%40massarray-system-1%4020142485
    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


    Comparison of allele frequencies 1 estimated using high-throughput sequencing vs. genotyping for 43 SNPs across two pools of 75 dairy cattle divergent for calving interval (CIV) . 1 Actual genotype frequencies calculated from Sequenom ® MassARRAY data obtained from previous studies [ , , , , ].

    Journal: BMC Genomics

    Article Title: Polymorphism discovery and allele frequency estimation using high-throughput DNA sequencing of target-enriched pooled DNA samples

    doi: 10.1186/1471-2164-13-16

    Figure Lengend Snippet: Comparison of allele frequencies 1 estimated using high-throughput sequencing vs. genotyping for 43 SNPs across two pools of 75 dairy cattle divergent for calving interval (CIV) . 1 Actual genotype frequencies calculated from Sequenom ® MassARRAY data obtained from previous studies [ , , , , ].

    Article Snippet: Estimated allele frequencies of a selection of SNPs from the sequence capture target enrichment and sequencing of pooled samples were compared to actual allele frequencies generated using Sequenom ® MassARRAY iPLEXTM gold assay.

    Techniques: Comparison, Next-Generation Sequencing

    Comparison between allele frequencies generated using Sequenom ®  MassARRAY  and Illumina GAIIx technologies.

    Journal: BMC Genomics

    Article Title: Polymorphism discovery and allele frequency estimation using high-throughput DNA sequencing of target-enriched pooled DNA samples

    doi: 10.1186/1471-2164-13-16

    Figure Lengend Snippet: Comparison between allele frequencies generated using Sequenom ® MassARRAY and Illumina GAIIx technologies.

    Article Snippet: Estimated allele frequencies of a selection of SNPs from the sequence capture target enrichment and sequencing of pooled samples were compared to actual allele frequencies generated using Sequenom ® MassARRAY iPLEXTM gold assay.

    Techniques: Comparison, Generated

    Sequencing traces of NESP55 gene for genomic DNA and cDNA from both maternal and foetal tissues . The genomic DNA from the mother of each foetus allowed genotyping of the maternal genotype, while the genomic DNA from each foetus allowed genotyping of the each foetus. Arrows indicate the exonic SNP, denoted R (A/G), which was used for both DNA genotyping and to analyse allele-specific expression status of NESP55 transcripts (cDNA) across tissues from 8 and 10 weeks old foetuses. Column number 4 presents the genotypes for all samples/animals tested. Column 5 indicates whether monoallelic ( i.e . uniparental) expression was detected.

    Journal: BMC Genetics

    Article Title: DNA sequence polymorphisms within the bovine guanine nucleotide-binding protein Gs subunit alpha (Gsα)-encoding ( GNAS ) genomic imprinting domain are associated with performance traits

    doi: 10.1186/1471-2156-12-4

    Figure Lengend Snippet: Sequencing traces of NESP55 gene for genomic DNA and cDNA from both maternal and foetal tissues . The genomic DNA from the mother of each foetus allowed genotyping of the maternal genotype, while the genomic DNA from each foetus allowed genotyping of the each foetus. Arrows indicate the exonic SNP, denoted R (A/G), which was used for both DNA genotyping and to analyse allele-specific expression status of NESP55 transcripts (cDNA) across tissues from 8 and 10 weeks old foetuses. Column number 4 presents the genotypes for all samples/animals tested. Column 5 indicates whether monoallelic ( i.e . uniparental) expression was detected.

    Article Snippet: All SNP genotyping was performed commercially by Sequenom Inc. (San Diego, CA, USA; http://www.sequenom.com using their proprietary MassARRAY iPLEXTM Gold genotyping platform.

    Techniques: Sequencing, Expressing