Thermo Fisher Scientific provides innovative products, tools, and resources that help advance the work of researchers via microarray analysis. Application areas that benefit from such an approach include plant and animal genomics and transcriptomics, including basic research and industrial applications of technologies for breeding, population diversity, trait analysis, and more. Unique solutions are also available for cancer research from discovery to clinical research and analytical validation. Microarray solutions are used in reproductive health research for prenatal, postnatal and carrier screening to understand genetic risk factors. The genetics of human complex traits, Mendelian disorders, and populations are also applications that can be advanced with Applied Biosystems microarray analysis, including through population-optimized and application-optimized genotyping to enable human genetic research workflows.
Predictive genomics research provides genetic perspectives to help predict disease risk and understand drug response to focus health care resources on improving outcomes and managing costs.
Reproductive health research for prenatal, postnatal, and newborn screening leads to a better understanding of genetic risk factors, providing scientific insight into the determination of reproductive options for planning or growing a family.
Agrigenomics genotyping solutions provide breeders and researchers with powerful and flexible genotyping tools to cost-effectively identify, verify, and screen complex genetic traits in plants and animals.
Microarray technology in the lab
Microarray technology enables the high-throughput analysis of genotyping, gene expression, and chromosome copy number variations and can be applied to various applications such as predictive genomics.
Microarray analysis solutions
Designing the best genotyping panel for your studies doesn’t need to be challenging or time-consuming. Axiom myDesign custom genotyping arrays offer extensive customization options with fast turnaround times for individual researchers or consortia who need specialized content.
Microarray based assays for molecular cytogenetics research provide a genome-wide reliable approach that enables high resolution DNA copy number analysis. CytoScan cytogenetics suite and Chromosome Analysis Software (ChAS) quickly and easily identify aneuploidies, microdeletions, microduplications, as well as other types of chromosomal aberrations across the genome.
The Axiom Genotyping Solution offers a uniquely flexible choice of customizable arrays or pre-designed arrays with imputation-aware designs covering more populations than any other technology.
Applied Biosystems agrigenomic genotyping solutions provide breeders and researchers with a powerful and flexible range of genotyping tools to cost-effectively identify, verify, and screen complex genetic traits in plants and animals.
Transcriptome-wide analysis can be complex. Matching your experimental requirements to the most appropriate tool can streamline your study, thereby reducing time to results and simplifying analysis. Expression microarrays simultaneously measure expression levels of thousands of RNA transcripts. For a fast path to important insights, even from challenging and precious samples, power your expression studies with Applied Biosystems expression arrays and assays.
An instrument for expression and genotyping experiments that seamlessly integrates hybridization, washing, and imaging in a single instrument to provide automated array processing—whether you are performing basic or applied research
The GeneChip Scanner 3000 7G System allows you to scan next-generation higher-density arrays, including SNP arrays with up to 900,000 SNPs, tiling arrays for transcription, and all-exon arrays.
A whole-genome microarray solution with hybrid design, both SNPs and non-polymorphic probes, providing broad coverage and high performance for detecting chromosomal aberrations with greater than 99% sensitivity
The new, high-throughput Axiom Propel workflow will help you easily scale-up genotyping to process millions of samples annually. Leave your mark on the future of predictive genomics. Propel your operations to new heights.
For Research Use Only. Not for use in diagnostic procedures.