Featured Solutions
Cancer Research Solutions from Thermo Fisher Scientific in Dubai
Unique solutions are available for cancer research, spanning from discovery to clinical validation, including cytogenetic studies of constitutional and cancer disorders. Additionally, the genetics of human complex traits, Mendelian disorders, and population studies can benefit from microarray analysis. This technology, through population-optimized and application-optimized genotyping, enhances human genetic research workflows.
GeneTitan™ Multi-Channel (MC) Instrument
Transform your lab with a GeneTitan™ instrument and experience the superior power of streamlining array processing for discovery, exploration, and screening. Both the GeneTitan Instrument for expression applications and the GeneTitan™ Multi-Channel (MC) Instrument for expression and genotyping seamlessly integrate hybridization, washing, and imaging in a single instrument to provide automated array processing—whether you are performing basic or applied research.
Axiom Biobank™ Genotyping Solution
The Applied Biosystems™ Axiom™ Biobank Genotyping Solution is the platform of choice for large-scale genotyping studies. Scientists from many of the world’s largest population genetics epidemiology projects have chosen Thermo Fisher Scientific as their partner to tailor the array design for their studies. The Axiom™ Biobank Genotyping Solution offers a cost-effective and comprehensive platform for all stages of research.
Pharmacogenomics
The Applied Biosystems™ PharmacoScan Solution™ offers broad coverage of industry-relevant, multiethnic content, and the capability to address markers in complex genes on the array-plate platform that has superior lot-to-lot reproducibility. The PharmacoScan Solution targets functional variations in all the key genes involved in the absorption, distribution, metabolism, and excretion (ADME) of commonly prescribed medication that can help reduce the lengthy timelines and complexities within the drug discovery process. The PharmacoScan Array plates are processed in the GeneTitan™ MC Instrument.
CarrierScan™ Assay
The Applied Biosystems™ CarrierScan™ Assay is an innovative, comprehensive, and high-throughput microarray-based tool for the reliable and robust detection of sequence and structural variation of preconception expanded carrier screening research across a wide range of ethnicities. The unique feature of this tool is the ability to consolidate multiple copy number and genotyping tests into a single molecular assay.
OncoScan CNV Assays
The genomes of cancer cells often contain changes in their chromosomal architecture and such alterations can be critical to tumor formation and growth progression. Understanding the copy number makeup of solid tumors provides valuable insights into tumor biology, evolution, and resistance to therapy. Studying chromosomal abnormalities and genomic instability is therefore key to fully profiling solid tumors and identifying potentially prognostic and predictive biomarkers.
Axiom™ Microbiome Array
The Axiom™ Microbiome Array researchers to detect all known microorganisms in a sample with a single assay. Designed in collaboration with the Lawrence Livermore National Library, the Axiom Microbiome Array provides species- and strain- level detection on a scalable platform with straightforward, easy-to-use software.
Axiom™ Precision Medicine Array
The Applied Biosystems™ Axiom™ Precision Medicine Research Array (PMRA) delivers a cost effective, broad population screening platform with proven clinical research utility. Powered by the Axiom Genotyping Solution and used by biobanks worldwide, the Axiom PMRA includes carefully selected, clinically significant pathogenic variants including those implicated for actionable genetic risks across a wide range of populations.
Clariom™ D Solution
Accelerate your biomarker research with the Applied Biosystems™ Clariom™ D Solutions, which offer the next generation of transcriptome-level profiling tools. The Clariom D solutions provide a highly detailed view of the transcriptome for a faster path to biomarker discovery.
Predictive Genomics
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. Thermo Fisher Scientific in Dubai provides solutions for both research goals, including specific microarray tools that are designed to enhance our understanding of complex diseases such as cancer and cardiovascular disease.
GeneTitan™ Multi-Channel (MC) Instrument
Transform your lab with a GeneTitan™ instrument and experience the superior power of streamlining array processing for discovery, exploration, and screening. Both the GeneTitan Instrument for expression applications and the GeneTitan™ Multi-Channel (MC) Instrument for expression and genotyping seamlessly integrate hybridization, washing, and imaging in a single instrument to provide automated array processing—whether you are performing basic or applied research.
Axiom Biobank™ Genotyping Solution
The Applied Biosystems™ Axiom™ Biobank Genotyping Solution is the platform of choice for large-scale genotyping studies. Scientists from many of the world’s largest population genetics epidemiology projects have chosen Thermo Fisher Scientific as their partner to tailor the array design for their studies. The Axiom™ Biobank Genotyping Solution offers a cost-effective and comprehensive platform for all stages of research.
Pharmacogenomics
The Applied Biosystems™ PharmacoScan Solution™ offers broad coverage of industry-relevant, multiethnic content, and the capability to address markers in complex genes on the array-plate platform that has superior lot-to-lot reproducibility. The PharmacoScan Solution targets functional variations in all the key genes involved in the absorption, distribution, metabolism, and excretion (ADME) of commonly prescribed medication that can help reduce the lengthy timelines and complexities within the drug discovery process. The PharmacoScan Array plates are processed in the GeneTitan™ MC Instrument.
CarrierScan™ Assay
The Applied Biosystems™ CarrierScan™ Assay is an innovative, comprehensive, and high-throughput microarray-based tool for the reliable and robust detection of sequence and structural variation of preconception expanded carrier screening research across a wide range of ethnicities. The unique feature of this tool is the ability to consolidate multiple copy number and genotyping tests into a single molecular assay.
OncoScan CNV Assays
The genomes of cancer cells often contain changes in their chromosomal architecture and such alterations can be critical to tumor formation and growth progression. Understanding the copy number makeup of solid tumors provides valuable insights into tumor biology, evolution, and resistance to therapy. Studying chromosomal abnormalities and genomic instability is therefore key to fully profiling solid tumors and identifying potentially prognostic and predictive biomarkers.
Axiom™ Microbiome Array
The Axiom™ Microbiome Array researchers to detect all known microorganisms in a sample with a single assay. Designed in collaboration with the Lawrence Livermore National Library, the Axiom Microbiome Array provides species- and strain- level detection on a scalable platform with straightforward, easy-to-use software.
Axiom™ Precision Medicine Array
The Applied Biosystems™ Axiom™ Precision Medicine Research Array (PMRA) delivers a cost effective, broad population screening platform with proven clinical research utility. Powered by the Axiom Genotyping Solution and used by biobanks worldwide, the Axiom PMRA includes carefully selected, clinically significant pathogenic variants including those implicated for actionable genetic risks across a wide range of populations.
Clariom™ D Solution
Accelerate your biomarker research with the Applied Biosystems™ Clariom™ D Solutions, which offer the next generation of transcriptome-level profiling tools. The Clariom D solutions provide a highly detailed view of the transcriptome for a faster path to biomarker discovery.
Reproductive Health
Understanding genetic risk factors to determine an individual or couple’s reproductive health status is an essential part of family planning. Genetic testing, in consultation with a physician and genetic counselor, can provide valuable information for making informed decisions, especially those impacted by difficulties in conception or pregnancy, or risk factors, such as age, ethnicity, and family history.
GeneChip™ Scanner 3000 7G
The Applied Biosystems GeneChip Scanner 3000 7G is an extension of the GeneChip Scanner 3000 (GCS 3000) series that 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 for whole-genome analysis.
CytoScan™ HD Suite
The CytoScan HD Suite is a whole-genome microarray solution comprised of array, reagents, software, and instrument designed for both SNPs and non-polymorphic probes, providing broad coverage and high performance for detecting chromosomal aberrations with greater than 99% sensitivity.
OncoScan CNV Assays
The genomes of cancer cells often contain changes in their chromosomal architecture and such alterations can be critical to tumor formation and growth progression. Understanding the copy number makeup of solid tumors provides valuable insights into tumor biology, evolution, and resistance to therapy. Studying chromosomal abnormalities and genomic instability is therefore key to fully profiling solid tumors and identifying potentially prognostic and predictive biomarkers.
Chromosome Analysis Suite (ChAS)
Chromosome Analysis Suite is a software offering intuitive and flexible workflow for accurate analysis tailored for cytogenetics. ChAS was developed with input from leading experts and is customized for copy number and cytogenetics research analysis and reporting. ChAS enables you to view and summarize chromosomal aberrations across the genome. Chromosomal aberrations may include copy number gain or loss, mosaicism, or loss/absence of heterozygosity (LOH/AOH).
Agrigenomics
Agrigenomic solutions designed to deliver accurate and actionable data when you need it most Thermo Fisher Scientific is committed to providing instruments, reagents, and solutions for plant and animal genotyping applications: simple, scalable, and affordable next-generation solutions that will help drive remarkable agricultural innovations. These solutions enable producers to develop healthier, more efficient crops and livestock to help nourish the world’s growing population.
GeneTitan™ Multi-Channel (MC) Instrument
Transform your lab with a GeneTitan™ instrument and experience the superior power of streamlining array processing for discovery, exploration, and screening. Both the GeneTitan Instrument for expression applications and the GeneTitan™ Multi-Channel (MC) Instrument for expression and genotyping seamlessly integrate hybridization, washing, and imaging in a single instrument to provide automated array processing—whether you are performing basic or applied research.
Axiom™ Genotyping Solution
The Axiom Genotyping Solution for agrigenomics provide breeders and researchers with powerful genotyping tools to identify, validate, and screen complex genetic traits in plants or animals. It includes arrays with genotype-tested content from the Axiom Genomic Database or de novo markers that are important to you. The complete solution comprises genotyping arrays, reagent kits, a fully automated workflow, and easy-to-use free data analysis tools.