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Massarray typer software v4

Manufactured by Labcorp
Sourced in United States

The MassArray TYPER software v4.0 is a tool designed for the analysis and interpretation of data generated by the MassArray system, a high-throughput genotyping platform. The software provides automated data processing and reporting capabilities to support genetic analysis workflows.

Automatically generated - may contain errors

3 protocols using massarray typer software v4

1

Genetic Variants in IL12A Associated with Primary Biliary Cholangitis

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Based on GWAS results of the European and Japanese PBC cohorts, we selected the most relevant 22 tag SNPs, at the chromosomal region (chr3:159619322–159800889) surrounding IL12A, from the 1000 Genomes Project for Asian populations with minor allele frequency >2% by Haploview v4.2.31 (link) The selected 22 SNPs around the genomic region of IL12A were genotyped in a cohort of Chinese Han individuals (586 cases/726 controls) by MassArray iPLEX.
The genomic DNA of each sample was extracted using a QIAamp DNA mini kit (Qiagen, Hilden, Germany), and SNP genotyping was performed by the MassArray iPLEX system (Sequenom, San Diego, CA, USA) at Beijing DNALead Co. LTD. All procedures were performed according to the manufacturer's instructions. Approximately 10 ng of genomic DNA was amplified by multiplex polymerase chain reaction (PCR) and the amplicons were subjected to locus-specific single-base extension reactions. The extended products were desalted and transferred to a 384-element SpectroCHIP array. Allele detection was performed using MALDI-TOF mass spectrometry, and the mass spectrograms were analyzed by the MassArray TYPER software v4.0 (Sequenom).
The procedures for SNP genotyping and Hardy–Weinberg equilibrium analysis were performed as previously reported.32 (link)
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2

Genotyping of Alzheimer's Disease Cohorts

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The France_AD cohort was genotyped with the with Illumina Human 610-Quad BeadChips. The Belgium_AD cohort was genotyped only for markers rs6455128 and rs7989332 by Sequenom MassARRAY assay using iPLEX Gold chemistry (Sequenom, Hamburg, Germany), followed by MALDI-TOF mass spectrometry. Polymerase chain reaction and extension primers were designed using MassARRAY Assay Design software v3.0.2.0 (Sequenom). Genotypes were called both automatically using MassARRAY Typer software v4.0 (Sequenom) and manually, blinded for disease status. The USA_AD cohort was genotyped only for markers rs6455128 and rs7989332 using TaqMan (Applied Biosystems) technology, according to established protocols. The GERAD samples (USA2_AD, UK_AD, and Germany_AD cohorts) were genotyped by Illumina 610-quad chip (data for 3333 cases and 1225 elderly screened controls) and by Illumina HumanHap550 Beadchip (data for 5235 population controls).
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3

SNP Genotyping of HELZ2 in Chinese Han

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The genomic DNA of each sample was extracted using QIAamp DNA mini kit (Qiagen, German), and SNP genotyping was performed by the MassArray iPLEX system (Sequenom, USA) at Beijing DnaLead Co. LTD. All procedures were performed according to the manufacturer’s instructions. Approximately 10 ng of genomic DNA was amplified by multiplex PCR and the amplicons subjected to locus-specific single-base extension reactions. The extended products were desalted and transferred to a 384-element SpectroCHIP array. Allele detection was performed using MALDI-TOF mass spectrometry, and the mass spectrograms were analyzed by the MassArray TYPER software v4.0 (Sequenom, USA). 6 SNPs in the coding sequence of HELZ2 were selected for genotyping in the 2 cohorts of Chinese Han (385 cases/726 controls and 201 cases/726 controls) by MassArray iPLEX.
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