Infinium 유전형 분석 어레이는 신뢰할 수 있는 데이터 품질과 귀중한 유전체 영역의 탁월한 커버리지로 주요 기관에서 고처리량 스크리닝 및 대규모 연구 프로그램을 위해 선택하는 플랫폼입니다. Infinium 기술은 탁월한 데이터 품질과 콜 비율, 일관적인 재현성을 제공합니다. Infinium은 SNP 복잡성 및 샘플 처리량을 기반으로 광범위한 마이크로어레이 옵션을 제공합니다.

Infinium 메틸레이션 기술을 통해 유전체의 메틸화 수치를 매우 정확하고 정밀하게 정량화할 수 있습니다. Infinium 메틸레이션 assay를 사용하여 단일 CpG 영역 수준에서 사이토신 메틸레이션를 검출하세요.
프로모션
Read how scientists are using arrays to further their genomic research across a diverse field of applications.
Read how Dr Benjamin Darbro at the University of Iowa Carver College of Medicine, uses a wide range of cytogenetic tools, including microarrays and more, to explore gene networks involved in neurodevelopmental disorders.
In this research paper, scientists make significant contributions to a better understanding of the genetic structure and production potential of Eşme sheep to optimize and inform breeding programs.
In this spotlight, Dr Kathleen Barnes talks about how genetic factors can influence disease in populations as well as factors influencing its global distribution using methylation arrays.
Find the right microarray or library prep kit for your needs. Filter by method, species, and more. Compare, share, and order kits.
Learn about the Infinium array product line that provide solutions for unparalleled genomic access and accuracy to detect genetic and epigenetic variation.
See how scientists developed a new multi-species platform based on the Illumina Infinium II array chemistry targeting approximately 3000 SNPs in wheat, oat and barley.
Watch how a mouse DNA methylation array can accelerate high sample-throughput studies in this important model organism.
SIllumina microarrays offer high-quality data and exceptional genomic coverage to propel genomic studies of any size.
Human genotyping arrays are ideal for processing thousands of samples to identify variants associated with traits and disease.
Methylation arrays enable high-throughput, quantitative interrogation of methylation sites across the genome at single-nucleotide resolution.
Software tools for array experimental design, sample tracking, and analysis of microarray data.
In this research paper, scientists investigate genes and variants underlying metabolic dysfunction-associated fatty liver diseases in a Korean adult population at a genome-wide level.
Scientists show that chromosomal microarray analysis can enhance the prenatal diagnostic accuracy by detecting submicroscopic copy number variants not visible with conventional methods.
Read how researchers used SNP array profiling to gain a better understanding of breast cancer etiology to facilitate predictive therapies and improve prognostic assessments.