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INFINIUM Inc human 660w-quad snp microarray platform
Human 660w Quad Snp Microarray Platform, supplied by INFINIUM Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/microarray+platform+infinium+arrays/660w+snp+array/pmc03280307-92-6-5
Average 90 stars, based on 1 article reviews
human 660w-quad snp microarray platform - by Bioz Stars, 2026-11
90/100 stars

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Related Articles

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Article Title: An Investigation of Genome-Wide Studies Reported Susceptibility Loci for Ulcerative Colitis Shows Limited Replication in North Indians
Article Snippet: 648 UC cases and 850 controls were genotyped using Infinium Human 660W-quad.

Article Title: Changes in Refractive Error During Young Adulthood: The Effects of Longitudinal Screen Time, Ocular Sun Exposure, and Genetic Predisposition.
Article Snippet: Samples from 1592 participants were analyzed in 2010 using an Infinium HD Human 660W-Quad BeadChip Array and those from an additional 310 participants were analyzed in 2013 using an Infinium OmniExpress-24 BeadChip Array.

Article Title: An Investigation of Genome-Wide Studies Reported Susceptibility Loci for Ulcerative Colitis Shows Limited Replication in North Indians
Article Snippet: Six of the 59 meta-analysis index SNPs were not present in the Infinium Human 660W-quad array used in this study ( ).


Article Title: An Investigation of Genome-Wide Studies Reported Susceptibility Loci for Ulcerative Colitis Shows Limited Replication in North Indians
Article Snippet: For replicating meta-analysis based associations, 648 cases and 850 controls were genotyped using Infinium Human 660W-quad.

Article Title: Association of AFF3 Gene Polymorphism rs10865035 with Rheumatoid Arthritis: A Population-Based Case-Control Study on a Pakistani Cohort
Article Snippet: They selected 42 candidate genes/loci (3 Asian and 39 European) and tested 603 SNPs, which were either index SNPs or were surrogate SNPs, using Infinium Human 660w-quad microarray methods for genotyping.

GWAS:

Article Title: Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism.
Article Snippet: .. GWAS was conducted in the complete dataset of 212 incident VTE families genotyped using the Infinium 660W SNP array. ..

Article Title: Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism.
Article Snippet: .. In the past several years, numerousGWAS have confirmed established risk factors, such as FV, FGG, and the ABO locus, and yielded novel susceptibility genes for VTE in adults.7-11 Here we present the first GWAS on VTE in children using the Infinium 660W SNP array and a large collection of affected nuclear families comprising 212 parentchild trios. ..



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