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Infinium hd ultra protocol

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The Infinium HD Ultra protocol is a laboratory equipment product designed for high-throughput genotyping. It provides a streamlined workflow for DNA sample preparation and analysis. The core function of this protocol is to enable efficient and accurate genotyping of genetic variants across the genome.

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Lab products found in correlation

Humanexome beadchip 12v1 a, by Illumina (2 mentions)

Spelling variants of this product

Infinium HD Assay Ultra Protocol (17 citations) Infinium HD Assay Ultra Protocol Guide (5 citations)

2 protocols using infinium hd ultra protocol

1

Exome Array Genotyping of HUNT Cohort

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We attempted genotyping of 5,771 HUNT individuals at the Genomic Core Facility, Norwegian University of Science and Technology, Norway, using the HumanExome-12v1_A Beadchip (Illumina, CA) and the Infinium HD ultra protocol. The exome array includes 247,870 markers focused on protein-altering variants (nonsynonymous, splicing, and stop-altering) selected from >12,000 exome and genome sequences, including variants associated with complex traits in previous GWAS, HLA tags, ancestry-informative markers, markers for identity-by-descent estimation, and random synonymous SNPs. Details about SNP content and selection strategies can be found at the exome array design webpage.
Holmen O.L., Zhang H., Fan Y., Hovelson D.H., Schmidt E.M., Zhou W., Guo Y., Zhang J., Langhammer A., Løchen M.L., Ganesh S.K., Vatten L., Skorpen F., Dalen H., Zhang J., Pennathur S., Chen J., Platou C., Mathiesen E.B., Wilsgaard T., Njølstad I., Boehnke M., Chen Y.E., Abecasis G.R., Hveem K, & Willer C.J. (2014). Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk. Nature genetics, 46(4), 345-351.
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2

Exome Array Genotyping of HUNT Cohort

Check if the same lab product or an alternative is used in the 5 most similar protocols
We attempted genotyping of 5,771 HUNT individuals at the Genomic Core Facility, Norwegian University of Science and Technology, Norway, using the HumanExome-12v1_A Beadchip (Illumina, CA) and the Infinium HD ultra protocol. The exome array includes 247,870 markers focused on protein-altering variants (nonsynonymous, splicing, and stop-altering) selected from >12,000 exome and genome sequences, including variants associated with complex traits in previous GWAS, HLA tags, ancestry-informative markers, markers for identity-by-descent estimation, and random synonymous SNPs. Details about SNP content and selection strategies can be found at the exome array design webpage.
Holmen O.L., Zhang H., Fan Y., Hovelson D.H., Schmidt E.M., Zhou W., Guo Y., Zhang J., Langhammer A., Løchen M.L., Ganesh S.K., Vatten L., Skorpen F., Dalen H., Zhang J., Pennathur S., Chen J., Platou C., Mathiesen E.B., Wilsgaard T., Njølstad I., Boehnke M., Chen Y.E., Abecasis G.R., Hveem K, & Willer C.J. (2014). Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk. Nature genetics, 46(4), 345-351.
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