Illumina Infinium

GPTKB entity

Statements (55)
Predicate Object
gptkbp:instance_of gptkb:physicist
gptkbp:bfsLayer 4
gptkbp:bfsParent gptkb:ILMN
gptkbp:applies_to genetic research
clinical diagnostics
pharmacogenomics
gptkbp:based_on bead array technology
gptkbp:developed_by gptkb:Illumina,_Inc.
gptkbp:enables large-scale studies
gptkbp:first_introduced gptkb:2005
https://www.w3.org/2000/01/rdf-schema#label Illumina Infinium
gptkbp:integrates_with Illumina sequencing technologies
gptkbp:is_available_in various formats
gptkbp:is_compatible_with various sample types
Illumina's sequencing platforms
third-party analysis tools
gptkbp:is_known_for high throughput
cost-effectiveness
flexibility in design
gptkbp:is_often_used_in population genetics
cancer research
agricultural genomics
gptkbp:is_part_of Illumina's agricultural applications
Illumina's clinical applications
Illumina's genomic services
Illumina's genotyping solutions
Illumina's product portfolio
Illumina's research applications
gptkbp:is_recognized_by gptkb:Research_Institute
industry standards
regulatory bodies
gptkbp:is_supported_by gptkb:Database_Management_System
gptkb:document
customer support services
training resources
bioinformatics tools
gptkbp:is_used_by biotechnology companies
pharmaceutical companies
research institutions
gptkbp:is_used_for genotyping
gptkbp:is_used_in clinical trials
transcriptomics
metagenomics
genome-wide association studies (GWAS)
gptkbp:offers multi-sample analysis
gptkbp:provides high accuracy
high sensitivity
high specificity
high-throughput genotyping
genetic variant detection
gptkbp:recognizes insertions and deletions (indels)
single nucleotide polymorphisms (SN Ps)
copy number variations (CN Vs)
gptkbp:supports custom array designs
gptkbp:utilizes SNP arrays