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genotyping experiments with single nucleotide polymorphism (snp) arrays  (deCODE genetics Inc)

 
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    deCODE genetics Inc genotyping experiments with single nucleotide polymorphism (snp) arrays
    Genotyping Experiments With Single Nucleotide Polymorphism (Snp) Arrays, supplied by deCODE genetics 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/snp+array+experiments/genotyping/pmc07779038-10-9-37
    Average 90 stars, based on 1 article reviews
    genotyping experiments with single nucleotide polymorphism (snp) arrays - by Bioz Stars, 2026-10
    90/100 stars

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    Marker:

    Article Title: A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease
    Article Snippet: .. Multi-point sib-pair based linkage analysis was performed using a microsatellite marker set, and single-SNP association tests were performed using markers from the Illumina 1 M genotyping chip from deCODE Genetics, Inc. All analyses were performed separately within each ethnic group. ..

    other:

    Article Title: jMorp updates in 2020: large enhancement of multi-omics data resources on the general Japanese population
    Article Snippet: In the UK Biobank cohort, a total of 500,000 genotyping experiments with single nucleotide polymorphism (SNP) arrays were performed by 2018 , and now, whole-genome analyses of all participants of the UK Biobank are being conducted by deCODE genetics Inc. in Iceland and the Welcome Sanger Institute in the United Kingdom.

    Article Title: Does diabetes mellitus modify the association between 17q12 risk variant and prostate cancer aggressiveness?
    Article Snippet: Of these men, 616 were genotyped in collaboration with deCODE Genetics, Inc. in Rejkjavik, Iceland.

    Article Title: Genome-wide association study of platelet aggregation in African Americans
    Article Snippet: In GeneSTAR, genome-wide SNP genotyping was performed at deCODE Genetics, Inc. using the Human 1Mv1_C array from Illumina, Inc. with an average call rate per sample of 99.65 % (overall missing data rate = 0.35 %).

    Article Title: CHRNA5/CHRNA3 Locus Associates with Increased Mortality among Smokers.
    Article Snippet: CHRNA5/CHRNA3 Locus Associates with Increased Mortality among Smokers Henna Kupiainen, Mikko Kuokkanen, Jukka Kontto, Jarmo Virtamo, Veikko Salomaa, Ari Lindqvist, Maritta Kilpeläinen & Tarja Laitinen To cite this article: Henna Kupiainen, Mikko Kuokkanen, Jukka Kontto, Jarmo Virtamo, Veikko Salomaa, Ari Lindqvist, Maritta Kilpeläinen & Tarja Laitinen (2016): CHRNA5/CHRNA3 Locus Associates with Increased Mortality among Smokers, COPD: Journal of Chronic Obstructive Pulmonary Disease, DOI: 10.3109/15412555.2015.1049260 To link to this article: http://dx.doi.org/10.3109/15412555.2015.1049260

    Article Title: Whole genome analysis on the genetic backgrounds associated with the secondary failure to etanercept in patients with rheumatoid arthritis.
    Article Snippet: Objectives: Etanercept is effective for the treatment of rheumatoid arthritis (RA).. However, some of the patients eventually lose efficacy (secondary failure) despite the absence of neutralizing antibodies.. We aimed to explore single nucleotide polymorphisms (SNPs) associated with



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