信頼できるデータ品質と貴重なゲノム領域の卓越したカバレッジにより、Infiniumジェノタイピングアレイは、主要な機関によってハイスループットのスクリーニングと大規模研究プログラムのために選択されるプラットフォームになっています。Infiniumテクノロジーにより、卓越したデータ品質とコールレート、および一貫した再現性が実現します。SNPの複雑性とサンプルスループットに基づいて、幅広いマイクロアレイオプションを提供しています。

Infiniumメチル化テクノロジーにより、ゲノムにおけるメチル化レベルを非常に正確かつ高精度に定量化できます。Infiniumメチル化アッセイを使用して、単一CpG部位レベルでシトシンのメチル化を検出します。
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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.