chip array screening Search Results


global screening array v2 genotyping chip  (Illumina Inc)
90
Illumina Inc global screening array v2 genotyping chip
Global Screening Array V2 Genotyping 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/result/global screening array v2 genotyping chip/product/Illumina Inc
Average 90 stars, based on 1 article reviews
global screening array v2 genotyping chip - by Bioz Stars, 2026-04
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human asian screening array-24 + v 1.0 gene chip  (Illumina Inc)
90
Illumina Inc human asian screening array-24 + v 1.0 gene chip
Human Asian Screening Array 24 + V 1.0 Gene 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/result/human asian screening array-24 + v 1.0 gene chip/product/Illumina Inc
Average 90 stars, based on 1 article reviews
human asian screening array-24 + v 1.0 gene chip - by Bioz Stars, 2026-04
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high-density infinium asian screening array  (INFINIUM Inc)
90
INFINIUM Inc high-density infinium asian screening array
a Sample distribution and statistics by geography. The proportion of samples sequenced by whole-genome sequencing (WGS) and <t>those</t> <t>genotyped</t> by high-density Infinium Asian Screening Array <t>(ASA)</t> were marked in red and blue, respectively. b The number of SNV and INDEL variants identified in the WBBC cohort in five frequency bins: AC = 1, AC = 2, AC > 2 and AF < 0.005, 0.005 ≤ AF ≤ 0.05, and AF > 0.05. c The number of variants in 22 autosomes and X chromosome in the WBBC, 1000 Genome Project (1000G), gnomAD, and UK10K datasets. The horizontal bar plot shows the total number of variants in each of the four datasets. The individual dots and connected dots indicate each dataset and a combination of two or more datasets, respectively. Each vertical bar represents the number of variants in each dataset or overlapping variants in those datasets. d Functional annotations of all variants that were absent in dbSNP Build 151. The proportion of each category was filled with a different color. e The pie chart only displayed the variants in the coding and splicing regions (10 bp from exon-intron boundary). Source data are provided as a file.
High Density Infinium Asian Screening Array, 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/result/high-density infinium asian screening array/product/INFINIUM Inc
Average 90 stars, based on 1 article reviews
high-density infinium asian screening array - by Bioz Stars, 2026-04
90/100 stars
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microarray chip data illumina asian screening array beadchip  (Illumina Inc)
90
Illumina Inc microarray chip data illumina asian screening array beadchip
a Sample distribution and statistics by geography. The proportion of samples sequenced by whole-genome sequencing (WGS) and <t>those</t> <t>genotyped</t> by high-density Infinium Asian Screening Array <t>(ASA)</t> were marked in red and blue, respectively. b The number of SNV and INDEL variants identified in the WBBC cohort in five frequency bins: AC = 1, AC = 2, AC > 2 and AF < 0.005, 0.005 ≤ AF ≤ 0.05, and AF > 0.05. c The number of variants in 22 autosomes and X chromosome in the WBBC, 1000 Genome Project (1000G), gnomAD, and UK10K datasets. The horizontal bar plot shows the total number of variants in each of the four datasets. The individual dots and connected dots indicate each dataset and a combination of two or more datasets, respectively. Each vertical bar represents the number of variants in each dataset or overlapping variants in those datasets. d Functional annotations of all variants that were absent in dbSNP Build 151. The proportion of each category was filled with a different color. e The pie chart only displayed the variants in the coding and splicing regions (10 bp from exon-intron boundary). Source data are provided as a file.
Microarray Chip Data Illumina Asian Screening Array Beadchip, 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/result/microarray chip data illumina asian screening array beadchip/product/Illumina Inc
Average 90 stars, based on 1 article reviews
microarray chip data illumina asian screening array beadchip - by Bioz Stars, 2026-04
90/100 stars
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global screening array-48 + v3.0 bead chip  (Illumina Inc)
90
Illumina Inc global screening array-48 + v3.0 bead chip
a Sample distribution and statistics by geography. The proportion of samples sequenced by whole-genome sequencing (WGS) and <t>those</t> <t>genotyped</t> by high-density Infinium Asian Screening Array <t>(ASA)</t> were marked in red and blue, respectively. b The number of SNV and INDEL variants identified in the WBBC cohort in five frequency bins: AC = 1, AC = 2, AC > 2 and AF < 0.005, 0.005 ≤ AF ≤ 0.05, and AF > 0.05. c The number of variants in 22 autosomes and X chromosome in the WBBC, 1000 Genome Project (1000G), gnomAD, and UK10K datasets. The horizontal bar plot shows the total number of variants in each of the four datasets. The individual dots and connected dots indicate each dataset and a combination of two or more datasets, respectively. Each vertical bar represents the number of variants in each dataset or overlapping variants in those datasets. d Functional annotations of all variants that were absent in dbSNP Build 151. The proportion of each category was filled with a different color. e The pie chart only displayed the variants in the coding and splicing regions (10 bp from exon-intron boundary). Source data are provided as a file.
Global Screening Array 48 + V3.0 Bead 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/result/global screening array-48 + v3.0 bead chip/product/Illumina Inc
Average 90 stars, based on 1 article reviews
global screening array-48 + v3.0 bead chip - by Bioz Stars, 2026-04
90/100 stars
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snp genotyping microarray chip global screening array-24 v2 beadchip  (Illumina Inc)
90
Illumina Inc snp genotyping microarray chip global screening array-24 v2 beadchip
a Sample distribution and statistics by geography. The proportion of samples sequenced by whole-genome sequencing (WGS) and <t>those</t> <t>genotyped</t> by high-density Infinium Asian Screening Array <t>(ASA)</t> were marked in red and blue, respectively. b The number of SNV and INDEL variants identified in the WBBC cohort in five frequency bins: AC = 1, AC = 2, AC > 2 and AF < 0.005, 0.005 ≤ AF ≤ 0.05, and AF > 0.05. c The number of variants in 22 autosomes and X chromosome in the WBBC, 1000 Genome Project (1000G), gnomAD, and UK10K datasets. The horizontal bar plot shows the total number of variants in each of the four datasets. The individual dots and connected dots indicate each dataset and a combination of two or more datasets, respectively. Each vertical bar represents the number of variants in each dataset or overlapping variants in those datasets. d Functional annotations of all variants that were absent in dbSNP Build 151. The proportion of each category was filled with a different color. e The pie chart only displayed the variants in the coding and splicing regions (10 bp from exon-intron boundary). Source data are provided as a file.
Snp Genotyping Microarray Chip Global Screening Array 24 V2 Beadchip, 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/result/snp genotyping microarray chip global screening array-24 v2 beadchip/product/Illumina Inc
Average 90 stars, based on 1 article reviews
snp genotyping microarray chip global screening array-24 v2 beadchip - by Bioz Stars, 2026-04
90/100 stars
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global screening array genome-wide association screening (gwas) chip  (Johns Hopkins HealthCare)
90
Johns Hopkins HealthCare global screening array genome-wide association screening (gwas) chip
a Sample distribution and statistics by geography. The proportion of samples sequenced by whole-genome sequencing (WGS) and <t>those</t> <t>genotyped</t> by high-density Infinium Asian Screening Array <t>(ASA)</t> were marked in red and blue, respectively. b The number of SNV and INDEL variants identified in the WBBC cohort in five frequency bins: AC = 1, AC = 2, AC > 2 and AF < 0.005, 0.005 ≤ AF ≤ 0.05, and AF > 0.05. c The number of variants in 22 autosomes and X chromosome in the WBBC, 1000 Genome Project (1000G), gnomAD, and UK10K datasets. The horizontal bar plot shows the total number of variants in each of the four datasets. The individual dots and connected dots indicate each dataset and a combination of two or more datasets, respectively. Each vertical bar represents the number of variants in each dataset or overlapping variants in those datasets. d Functional annotations of all variants that were absent in dbSNP Build 151. The proportion of each category was filled with a different color. e The pie chart only displayed the variants in the coding and splicing regions (10 bp from exon-intron boundary). Source data are provided as a file.
Global Screening Array Genome Wide Association Screening (Gwas) Chip, supplied by Johns Hopkins HealthCare, 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/result/global screening array genome-wide association screening (gwas) chip/product/Johns Hopkins HealthCare
Average 90 stars, based on 1 article reviews
global screening array genome-wide association screening (gwas) chip - by Bioz Stars, 2026-04
90/100 stars
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gwas genotyping illumina global screening array chip  (Illumina Inc)
90
Illumina Inc gwas genotyping illumina global screening array chip
a Sample distribution and statistics by geography. The proportion of samples sequenced by whole-genome sequencing (WGS) and <t>those</t> <t>genotyped</t> by high-density Infinium Asian Screening Array <t>(ASA)</t> were marked in red and blue, respectively. b The number of SNV and INDEL variants identified in the WBBC cohort in five frequency bins: AC = 1, AC = 2, AC > 2 and AF < 0.005, 0.005 ≤ AF ≤ 0.05, and AF > 0.05. c The number of variants in 22 autosomes and X chromosome in the WBBC, 1000 Genome Project (1000G), gnomAD, and UK10K datasets. The horizontal bar plot shows the total number of variants in each of the four datasets. The individual dots and connected dots indicate each dataset and a combination of two or more datasets, respectively. Each vertical bar represents the number of variants in each dataset or overlapping variants in those datasets. d Functional annotations of all variants that were absent in dbSNP Build 151. The proportion of each category was filled with a different color. e The pie chart only displayed the variants in the coding and splicing regions (10 bp from exon-intron boundary). Source data are provided as a file.
Gwas Genotyping Illumina Global 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/result/gwas genotyping illumina global screening array chip/product/Illumina Inc
Average 90 stars, based on 1 article reviews
gwas genotyping illumina global screening array chip - by Bioz Stars, 2026-04
90/100 stars
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global screening array chip  (Genergy Biotechnology Co)
90
Genergy Biotechnology Co global screening array chip
a Sample distribution and statistics by geography. The proportion of samples sequenced by whole-genome sequencing (WGS) and <t>those</t> <t>genotyped</t> by high-density Infinium Asian Screening Array <t>(ASA)</t> were marked in red and blue, respectively. b The number of SNV and INDEL variants identified in the WBBC cohort in five frequency bins: AC = 1, AC = 2, AC > 2 and AF < 0.005, 0.005 ≤ AF ≤ 0.05, and AF > 0.05. c The number of variants in 22 autosomes and X chromosome in the WBBC, 1000 Genome Project (1000G), gnomAD, and UK10K datasets. The horizontal bar plot shows the total number of variants in each of the four datasets. The individual dots and connected dots indicate each dataset and a combination of two or more datasets, respectively. Each vertical bar represents the number of variants in each dataset or overlapping variants in those datasets. d Functional annotations of all variants that were absent in dbSNP Build 151. The proportion of each category was filled with a different color. e The pie chart only displayed the variants in the coding and splicing regions (10 bp from exon-intron boundary). Source data are provided as a file.
Global Screening Array Chip, supplied by Genergy Biotechnology Co, 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/result/global screening array chip/product/Genergy Biotechnology Co
Average 90 stars, based on 1 article reviews
global screening array chip - by Bioz Stars, 2026-04
90/100 stars
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asian screening array + multidisease-24 gene chip  (Illumina Inc)
90
Illumina Inc asian screening array + multidisease-24 gene chip
a Sample distribution and statistics by geography. The proportion of samples sequenced by whole-genome sequencing (WGS) and <t>those</t> <t>genotyped</t> by high-density Infinium Asian Screening Array <t>(ASA)</t> were marked in red and blue, respectively. b The number of SNV and INDEL variants identified in the WBBC cohort in five frequency bins: AC = 1, AC = 2, AC > 2 and AF < 0.005, 0.005 ≤ AF ≤ 0.05, and AF > 0.05. c The number of variants in 22 autosomes and X chromosome in the WBBC, 1000 Genome Project (1000G), gnomAD, and UK10K datasets. The horizontal bar plot shows the total number of variants in each of the four datasets. The individual dots and connected dots indicate each dataset and a combination of two or more datasets, respectively. Each vertical bar represents the number of variants in each dataset or overlapping variants in those datasets. d Functional annotations of all variants that were absent in dbSNP Build 151. The proportion of each category was filled with a different color. e The pie chart only displayed the variants in the coding and splicing regions (10 bp from exon-intron boundary). Source data are provided as a file.
Asian Screening Array + Multidisease 24 Gene 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/result/asian screening array + multidisease-24 gene chip/product/Illumina Inc
Average 90 stars, based on 1 article reviews
asian screening array + multidisease-24 gene chip - by Bioz Stars, 2026-04
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Image Search Results


a Sample distribution and statistics by geography. The proportion of samples sequenced by whole-genome sequencing (WGS) and those genotyped by high-density Infinium Asian Screening Array (ASA) were marked in red and blue, respectively. b The number of SNV and INDEL variants identified in the WBBC cohort in five frequency bins: AC = 1, AC = 2, AC > 2 and AF < 0.005, 0.005 ≤ AF ≤ 0.05, and AF > 0.05. c The number of variants in 22 autosomes and X chromosome in the WBBC, 1000 Genome Project (1000G), gnomAD, and UK10K datasets. The horizontal bar plot shows the total number of variants in each of the four datasets. The individual dots and connected dots indicate each dataset and a combination of two or more datasets, respectively. Each vertical bar represents the number of variants in each dataset or overlapping variants in those datasets. d Functional annotations of all variants that were absent in dbSNP Build 151. The proportion of each category was filled with a different color. e The pie chart only displayed the variants in the coding and splicing regions (10 bp from exon-intron boundary). Source data are provided as a file.

Journal: Nature Communications

Article Title: Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project

doi: 10.1038/s41467-022-30526-x

Figure Lengend Snippet: a Sample distribution and statistics by geography. The proportion of samples sequenced by whole-genome sequencing (WGS) and those genotyped by high-density Infinium Asian Screening Array (ASA) were marked in red and blue, respectively. b The number of SNV and INDEL variants identified in the WBBC cohort in five frequency bins: AC = 1, AC = 2, AC > 2 and AF < 0.005, 0.005 ≤ AF ≤ 0.05, and AF > 0.05. c The number of variants in 22 autosomes and X chromosome in the WBBC, 1000 Genome Project (1000G), gnomAD, and UK10K datasets. The horizontal bar plot shows the total number of variants in each of the four datasets. The individual dots and connected dots indicate each dataset and a combination of two or more datasets, respectively. Each vertical bar represents the number of variants in each dataset or overlapping variants in those datasets. d Functional annotations of all variants that were absent in dbSNP Build 151. The proportion of each category was filled with a different color. e The pie chart only displayed the variants in the coding and splicing regions (10 bp from exon-intron boundary). Source data are provided as a file.

Article Snippet: In addition, 6025 individuals were genotyped by high-density Infinium Asian Screening Array (ASA), including 184 individuals who were also whole-genome sequenced.

Techniques: Sequencing, Functional Assay