This chip analyzes more than 750,000 markers, and the chip points into the locations of common and rare diseases in clinical and disease studies related to the Southeast Asian population.
The sites are selected from a wide range of international public databases, including ClinVar, NHGRI-GWAS, CPIC, PharmaGKB and PharmaADME.
A
Application features:
★Variation points of GWAS
★Evidence markers for potential clinical relevance (pharmacogenomics, ClinVar, ACMG, exclusive markers)
★Immune-related markers (human leukocyte antigen, killer immunoglobulin-like receptor, autoimmunity and inflammation)
★Functional variation (loss of function, expression of quantitative trait loci, non-synonymous variants, lung phenotype)
★Disease-related mutations (Alzheimer's disease, cardiac metabolism, neurological disorders, diabetes, cancer mutations, heart mutations, other rare mutations)
★Used to track related variations (fingerprint and sample tracking, mitochondria, Y chromosome)
This chip analyzes more than 750,000 markers, and the chip points into the locations of common and rare diseases in clinical and disease studies related to the Southeast Asian population.
The sites are selected from a wide range of international public databases, including ClinVar, NHGRI-GWAS, CPIC, PharmaGKB and PharmaADME.
A
Application features:
★Variation points of GWAS
★Evidence markers for potential clinical relevance (pharmacogenomics, ClinVar, ACMG, exclusive markers)
★Immune-related markers (human leukocyte antigen, killer immunoglobulin-like receptor, autoimmunity and inflammation)
★Functional variation (loss of function, expression of quantitative trait loci, non-synonymous variants, lung phenotype)
★Disease-related mutations (Alzheimer's disease, cardiac metabolism, neurological disorders, diabetes, cancer mutations, heart mutations, other rare mutations)
★Used to track related variations (fingerprint and sample tracking, mitochondria, Y chromosome)
Precision Medicine Array
統計分析圖
用分析圖解決您的各種需求