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Ht 12 v3.0 arrays

Manufactured by Illumina
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The HT-12 V3.0 arrays are high-throughput gene expression microarray platforms designed and manufactured by Illumina. The arrays provide comprehensive genome-wide coverage, enabling the analysis of over 47,000 probes per sample. They are intended for use in gene expression profiling studies, allowing researchers to simultaneously measure the expression levels of thousands of genes in a single experiment.

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Lab products found in correlation

Omniquad array, by Illumina (2 mentions)

2 protocols using ht 12 v3.0 arrays

1

Population-based Cohort Study of Genetic and Transcriptomic Profiles

Cited 1 time
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n = 139 The Center for Health Discovery and Well Being (CD-HWB) Study24 (link) is a population based cohort consisting of 139 individuals of European descent collected in Atlanta USA. Gene expression profiles were generated with Illumina HT-12 V3.0 arrays from peripheral blood collected from Tempus tubes that preserve RNA. Whole genome genotypes were measured using Illumina OmniQuad arrays. Due to the small sample size, most SNP pairs did not pass filtering in this dataset (20 SNP pairs remained) and so we have excluded it from the rest of the analysis.
Hemani G., Shakhbazov K., Westra H.J., Esko T., Henders A.K., McRae A.F., Yang J., Gibson G., Martin N.G., Metspalu A., Franke L., Montgomery G.W., Visscher P.M, & Powell J.E. (2014). Detection and replication of epistasis influencing transcription in humans. Nature, 508(7495), 249-253.
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2

Population-based Cohort Study of Genetic and Transcriptomic Profiles

Cited 1 time
Check if the same lab product or an alternative is used in the 5 most similar protocols
n = 139 The Center for Health Discovery and Well Being (CD-HWB) Study24 (link) is a population based cohort consisting of 139 individuals of European descent collected in Atlanta USA. Gene expression profiles were generated with Illumina HT-12 V3.0 arrays from peripheral blood collected from Tempus tubes that preserve RNA. Whole genome genotypes were measured using Illumina OmniQuad arrays. Due to the small sample size, most SNP pairs did not pass filtering in this dataset (20 SNP pairs remained) and so we have excluded it from the rest of the analysis.
Hemani G., Shakhbazov K., Westra H.J., Esko T., Henders A.K., McRae A.F., Yang J., Gibson G., Martin N.G., Metspalu A., Franke L., Montgomery G.W., Visscher P.M, & Powell J.E. (2014). Detection and replication of epistasis influencing transcription in humans. Nature, 508(7495), 249-253.
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