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| Genome-wide genotyping data were produced using the Illumina HumanCNV370v1_C array platform and filtered using the following criteria: 1) per sample call rate ≥ 99%, 2) SNP minor allele frequency ≥ 1%, 3) SNP call rate ≥ 95%, 4) SNP HWE p-value ≥ 1x10 -6 , 5) removing unexpected relatives, resulting in a set of 324067 autosomal SNPs across 3307 unrelated samples (2157 cases and 1150 controls). |
| Genome-wide genotyping data were produced using the Illumina HumanCNV370v1_C array platform and filtered using the following criteria: 1) per sample call rate ≥ 98%, 2) SNP minor allele frequency ≥ 1%, 3) SNP call rate ≥ 95%, 4) SNP HWE p-value ≥ 1x10 -6 , 5) less than two SNP duplicate errors, 6) less than three SNP parent-parent-child trio errors, resulting in a set of 333313 SNPs across 3309 unrelated samples. Genome-wide association scan has been pre-computed by NCBI . |
| Genome-wide genotyping data were produced using the Illumina HumanCNV370v1_C array platform and filtered using the following criteria: 1) per sample call rate ≥ 98%, 2) SNP minor allele frequency ≥ 1%, 3) SNP call rate ≥ 95%, 4) SNP HWE p-value ≥ 1x10 -6 , 5) less than two SNP duplicate errors, 6) less than three SNP parent-parent-child trio errors, resulting in a set of 333313 SNPs across 3309 unrelated samples. Genome-wide association scan has been pre-computed by NCBI . |
| Genome-wide genotyping data were produced using the Illumina HumanCNV370v1_C array platform and filtered using the following criteria: 1) per sample call rate ≥ 99%, 2) SNP minor allele frequency ≥ 1%, 3) SNP call rate ≥ 95%, 4) SNP HWE p-value ≥ 1x10 -6 , 5) removing unexpected relatives, resulting in a set of 324067 autosomal SNPs across 3307 unrelated samples (2157 cases and 1150 controls). |