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Genomestudio genotyping analysis module v1

Manufactured by Illumina

The GenomeStudio Genotyping Analysis Module v1.8.4 is a software application designed for the analysis of genetic data generated from Illumina's microarray platforms. It provides a comprehensive suite of tools for the processing, visualization, and interpretation of genotyping data. The module enables users to perform tasks such as data quality control, genotype calling, and association analyses.

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2 protocols using genomestudio genotyping analysis module v1

1

SNP Genotyping of DH Populations

Check if the same lab product or an alternative is used in the 5 most similar protocols

Example 3

The three DH populations, YSC, YDN, and TN, were genotyped with 12,000 SNP markers developed at DAS on two Illumina Infinium chips on the BeadStation 500 G per manufacturer's protocol (Illumina, San Diego, Calif.). Genotypic data was analyzed using the GenomeStudio Genotyping Analysis Module v1.8.4 (Illumina, San Diego, Calif.), which converts fluorescent signals for each SNP into A and B signals whose values reflect the relative abundance of arbitrarily assigned A and B alleles. Signal is converted into polar coordinates, using the Manhattan distance metric for the intensity R, and with Theta∈[0,1] representing angle ∈[0,90] degrees. Each marker is clustered in Cartesian coordinates, and the genotypes {AA, AB, BB} are assigned to samples in clusters close to Theta-{0, ½, 1}.

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2

SNP Genotyping of DH Populations

Check if the same lab product or an alternative is used in the 5 most similar protocols

Example 3

The three DH populations, YSC, YDN, and TN, were genotyped with 12,000 SNP markers developed at DAS on two Illumina Infinium chips on the BeadStation 500 G per manufacturer's protocol (Illumina, San Diego, Calif.). Genotypic data was analyzed using the GenomeStudio Genotyping Analysis Module v1.8.4 (Illumina, San Diego, Calif.), which converts fluorescent signals for each SNP into A and B signals whose values reflect the relative abundance of arbitrarily assigned A and B alleles. Signal is converted into polar coordinates, using the Manhattan distance metric for the intensity R, and with Theta∈[0,1] representing angle∈[0,90] degrees. Each marker is clustered in Cartesian coordinates, and the genotypes {AA, AB, BB} are assigned to samples in clusters close to Theta={0, ½, 1}.

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