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asian screening array chip  (Illumina Inc)


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    Illumina Inc asian screening array chip
    Asian Screening Array Chip, supplied by Illumina 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/chip+array+screening/global+screening+array+chips/pmc12106753-320-6-10
    Average 90 stars, based on 1 article reviews
    asian screening array chip - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Novel functional eQTL-SNPs associated with susceptibility to occupational pulmonary fibrosis: A multi-stage study.
    Article Snippet: Genome-wide genotyping was accomplished using a high-throughput genotyping chip (Illumina Asian screening array chip) with 746,113 SNPs designed for Asian populations.

    Article Title: A non-coding variant linked to metabolic obesity with normal weight affects actin remodelling in subcutaneous adipocytes
    Article Snippet: Genotyping was performed using the Illumina Global Screening bead-chip array.

    Article Title: Genetic legacy of ancient hunter-gatherer Jomon in Japanese populations
    Article Snippet: The subjects were genotyped using an Illumina Asian Screening Array chip.

    Article Title: Recommendations for Improving the Use of Direct-To-Consumer Genetic Testing Databases in Law Enforcement Investigations
    Article Snippet: Executive Summary: Prisoners are some of the most vulnerable populations in our society today, often relinquishing to the state everything from medical autonomy to family support.. In a system where wrongful convictions are not unheard of, it is critical that we preserve the civil rights of investigative subjects wherever possible.. Law enforcement agencies in the United States have increasingly begun using direct-to-consumer recreational genetic databases as a tool to enable forensic investigations.

    Article Title: Genetic influence on vascular smooth muscle cell apoptosis
    Article Snippet: DNA extracted from samples ( n = 2016) of the VSMC biobank was genotyped for 760,000 variants with the use of the Illumina Global Screening Array Multi-Diseases v2.0 bead-chips, followed by imputation to obtain genotypic information for 7,334,165 variants, as detailed previously [ ].

    Article Title: Whole-genome sequencing analyses suggest novel genetic factors associated with Alzheimer’s disease and a cumulative effects model for risk liability
    Article Snippet: Genomic DNA was genotyped using an Asian Screening Array Chip (Illumina).

    Control:

    Article Title: Whole-genome sequencing analyses suggest novel genetic factors associated with Alzheimer's disease and a cumulative effects model for risk liability.
    Article Snippet: .. Chip array data quality control Genomic DNA was genotyped using an Asian Screening Array Chip (Illumina). ..

    Sampling:

    Article Title: Distinct effects of early-stage and late-stage socioeconomic factors on brain and behavioral traits.
    Article Snippet: Socioeconomic status (SES) is a time-varying multidimensional construct with ill-defined dimension-specific and age-specific effects on brain and behavior.. We investigated these effects in 4,228 young adults.. From 16 socioeconomic indicators, assessed for early (0–10 years) and late (>10 years) stages, we constructed family, provincial, family adverse and neighborhood adverse socioeconomic dimensions.



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    INFINIUM Inc global screening array-24 v.30 gwas chip
    Genomic profiling of iPSC lines from African Somatic and Stem Cell Bank. A, Workflow. B–I, Genetic analyses of iPSC. B, PCA of common genetic variants measured in unique iPSC lines (gray, cohort) compared to 1000 Genomes reference: AFR, AMR, EAS, EUR, SAS. C, Frequency of APOE genotypes among iPSC lines. D–I, PRS. D–E, Distribution of PRS represented using reference (salmon, REF) and iPSC samples (cyan, TRG). G–H, Distribution of PRS represented based on Nigerian ethnic group. D, G, PRS for AD including the APOE gene locus. E, H, PRS for AD excluding the APOE gene locus. F, I, PRS for PD. J, PCA of transcriptomic data generated from iPSCs (500 most variable gene transcripts). K, XIST, expressed on the inactivated X‐chromosome, in iPSC lines. Graphs represent CPM mean ± SEM. ****, p < 0.0001. Blue, female. Red, male. AD, Alzheimer's disease; AFR, Africans; AMR, admixed Americans; APOE , apolipoprotein E; CPM, counts per million; EAS, East Asians; EUR, Europeans; <t>GWAS,</t> <t>genome‐wide</t> <t>association</t> <t>study;</t> iPSC, induced pluripotent stem cell; PCA, principal component analysis; PD, Parkinson's disease; PRS, polygenic risk score; REF, reference; SAS, South Asian; SEM, standard error of the mean.
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    Genomic profiling of iPSC lines from African Somatic and Stem Cell Bank. A, Workflow. B–I, Genetic analyses of iPSC. B, PCA of common genetic variants measured in unique iPSC lines (gray, cohort) compared to 1000 Genomes reference: AFR, AMR, EAS, EUR, SAS. C, Frequency of APOE genotypes among iPSC lines. D–I, PRS. D–E, Distribution of PRS represented using reference (salmon, REF) and iPSC samples (cyan, TRG). G–H, Distribution of PRS represented based on Nigerian ethnic group. D, G, PRS for AD including the APOE gene locus. E, H, PRS for AD excluding the APOE gene locus. F, I, PRS for PD. J, PCA of transcriptomic data generated from iPSCs (500 most variable gene transcripts). K, XIST, expressed on the inactivated X‐chromosome, in iPSC lines. Graphs represent CPM mean ± SEM. ****, p < 0.0001. Blue, female. Red, male. AD, Alzheimer's disease; AFR, Africans; AMR, admixed Americans; APOE , apolipoprotein E; CPM, counts per million; EAS, East Asians; EUR, Europeans; GWAS, genome‐wide association study; iPSC, induced pluripotent stem cell; PCA, principal component analysis; PD, Parkinson's disease; PRS, polygenic risk score; REF, reference; SAS, South Asian; SEM, standard error of the mean.

    Journal: Alzheimer's & Dementia

    Article Title: Somatic and Stem Cell Bank to study the contribution of African ancestry to dementia: African iPSC Initiative

    doi: 10.1002/alz.70145

    Figure Lengend Snippet: Genomic profiling of iPSC lines from African Somatic and Stem Cell Bank. A, Workflow. B–I, Genetic analyses of iPSC. B, PCA of common genetic variants measured in unique iPSC lines (gray, cohort) compared to 1000 Genomes reference: AFR, AMR, EAS, EUR, SAS. C, Frequency of APOE genotypes among iPSC lines. D–I, PRS. D–E, Distribution of PRS represented using reference (salmon, REF) and iPSC samples (cyan, TRG). G–H, Distribution of PRS represented based on Nigerian ethnic group. D, G, PRS for AD including the APOE gene locus. E, H, PRS for AD excluding the APOE gene locus. F, I, PRS for PD. J, PCA of transcriptomic data generated from iPSCs (500 most variable gene transcripts). K, XIST, expressed on the inactivated X‐chromosome, in iPSC lines. Graphs represent CPM mean ± SEM. ****, p < 0.0001. Blue, female. Red, male. AD, Alzheimer's disease; AFR, Africans; AMR, admixed Americans; APOE , apolipoprotein E; CPM, counts per million; EAS, East Asians; EUR, Europeans; GWAS, genome‐wide association study; iPSC, induced pluripotent stem cell; PCA, principal component analysis; PD, Parkinson's disease; PRS, polygenic risk score; REF, reference; SAS, South Asian; SEM, standard error of the mean.

    Article Snippet: Samples were analyzed by an Infinium Global Screening Array‐24 v.30 GWAS Chip.

    Techniques: Generated, GWAS