## TruSight Oncology 500 v2 Enable CGP with a large pan-cancer panel covering all main variant classes plus key biomarkers (TMB, MSI, and HRD) from FFPE tissue. [View product](https://www.illumina.com/products/by-type/clinical-research-products/trusight-oncology-500.html) ## TruSight Oncology 500 ctDNA v2 Enable CGP with a pan-cancer panel capable of detecting key IO gene signatures (TMB, MSI) plus all main variant classes from ctDNA in blood plasma. [View product](https://www.illumina.com/products/by-type/clinical-research-products/trusight-oncology-500-ctdna.html) ## [AmpliSeq for Illumina BRCA Panel](https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/ampliseq-brca-panel.html) Targeted research panel investigating somatic and germline variants in _BRCA1_ and _BRCA2_. Assay time: 5 hours (lib… Hands-on time: <1.5 hr Input quantity: 1–100 ng (10… ## [AmpliSeq for Illumina Cancer Hotspot Panel v2](https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/ampliseq-cancer-hotspot-panel.html) Targeted research panel investigating hotspot regions of 50 genes with known associations to cancer. Assay time: 5 hours (lib… Hands-on time: < 1.5 hr Input quantity: 1–100 ng (10… ## [AmpliSeq for Illumina Childhood Cancer Panel](https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/ampliseq-childhood-cancer-panel.html) Targeted panel for investigating 203 genes associated with cancer in children and young adults. Assay time: 5-6 hr (libr… Hands-on time: < 1.5 hr Input quantity: 10 ng high-q… ## [AmpliSeq for Illumina Comprehensive Panel v3](https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/ampliseq-comprehensive-panel.html) Targeted DNA and RNA research panel investigating variants across 161 genes associated with a range of cancer types. Assay time: 5-6 hr (libr… Hands-on time: <1.5 hr Input quantity: 1–100 ng (10… ## [AmpliSeq for Illumina Focus Panel](https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/ampliseq-focus-panel.html) Targeted DNA and RNA research panel investigating 52 genes with known relevance to solid tumors. Assay time: 5-6 hr (libr… Hands-on time: < 1.5 hr Input quantity: 1–100 ng (10… ## [AmpliSeq for Illumina Immune Repertoire Plus, TCR beta Panel](https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/ampliseq-immune-repertoire-panel.html) Targeted RNA research panel to investigate T cell diversity and clonal expansion by sequencing T cell receptor beta chain rearrangements. Assay time: 5.5 – 7.5 ho… Hands-on time: < 1.5 hr Input quantity: 10–1,000 ng ## [AmpliSeq for Illumina Immune Response Panel](https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/ampliseq-immune-response-panel.html) Targeted RNA expression panel investigating 395 genes involved in tumor-immune system interactions. Assay time: 6 hr (librar… Hands-on time: < 1.5 hr Input quantity: 1–100 ng (10… ## [AmpliSeq for Illumina Myeloid Panel](https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/ampliseq-myeloid-panel.html) Targeted panel to investigate 40 DNA genes, 29 RNA fusion driver genes, and 5 gene expression levels associated with myeloid cancers. Assay time: 5.5 – 7.5 ho… Hands-on time: < 1.5 hr Input quantity: 20 ng high-q… ## [AmpliSeq for Illumina On-Demand](https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/ampliseq-on-demand-panel.html) Tailor panel designs for human disease research efficiently and conveniently by selecting from a catalog of over 5,000 pretested genes. Assay time: As low as 5 … Hands-on time: 1.5 hr Input quantity: 1-100 ng DNA ## [COVIDSeq Assay (96 samples)](https://www.illumina.com/products/by-type/clinical-research-products/covidseq-assay.html) This low- to mid-throughput NGS assay enables labs of any size to identify and track the emergence and prevalence of novel SARS-CoV-2 variants. ## [COVIDSeq Test (RUO Version)](https://www.illumina.com/products/by-type/clinical-research-products/covidseq.html) This high-throughput NGS assay enables labs to detect SARS-CoV-2 mutations to identify and track the emergence and prevalence of novel variants. ## [Infinium CytoSNP-850K BeadChip](https://www.illumina.com/products/by-type/clinical-research-products/infinium-cytosnp-850k.html) A consortium-built SNP-based microarray providing thorough coverage of 3262 cytogenetically relevant genes for constitutional and cancer research. Sample throughput: 960 samples/… Number of samples: 8 samples pe… Number of markers: Fixed marker… ## [Infinium Global Clinical Research Array-24 v1.0 Kit](https://www.illumina.com/products/by-type/clinical-research-products/infinium-global-clinical-research.html) The Global Clinical Research Array offers exceptional coverage of key genome-wide clinical content with a highly scalable workflow. Sample throughput: 5760 Number of samples: 24 samples p… Number of markers: 1,157,992 ## [Infinium Global Diversity Array with Carrier Screening Content-8 v2.0 Kit](https://www.illumina.com/products/by-type/microarray-kits/infinium-global-diversity-array-carrier-screening.html) This high-performance microarray research kit provides a cost-effective, scalable workflow to support pan-ethnic carrier screening studies. Number of samples: 8 samples pe… ## [Infinium Global Diversity Array with Cytogenetics-8](https://www.illumina.com/products/by-type/clinical-research-products/infinium-global-diversity-array-cytogenetics-8.html) Profile clinical research variants associated with congenital disease, cancer research, pharmacogenomics (PGx), and exome content with this microarray. Number of samples: 8 samples pe… ## [Infinium Global Screening Array with Cytogenetics-24](https://www.illumina.com/products/by-type/clinical-research-products/infinium-global-screening-array-cytogenetics-24.html) Detect structural variation in the human genome and examine cytogenomic changes in constitutional diseases and cancers with this research microarray. Number of samples: 24 samples p… ## [Pillar oncoReveal Multi-Cancer RNA Fusion v2 Panel](https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/pillar-oncoreveal-multi-cancer-rna-fusion-panel.html) Targeted panel targeting 83 RNA fusions from FFPE tissue across multiple solid tumor types. Assay time: 48 hr from s… Hands-on time: ~3 hr Input quantity: 10–50 ng RNA ## [SurePlex DNA Amplification System](https://www.illumina.com/products/by-type/clinical-research-products/sureplex.html) Used to generate a DNA template from single cells. Ideal for use with PGS research applications. Assay time: ~3 hours Hands-on time: ~1 hr Input quantity: Single cell … ## [TG VeriSeq NIPT Sample Prep Kits (for research)](https://www.illumina.com/products/by-type/clinical-research-products/tg-veriseq-nipt.html) This kit is for the extraction, library preparation, and quantitation of cell-free DNA fragments isolated from maternal whole blood samples. ## [TruSight Cancer](https://www.illumina.com/products/by-type/clinical-research-products/trusight-cancer.html) These expert-defined sequencing research panels target 94 genes and 284 SNPs associated with a predisposition towards various cancers. Assay time: 1.5 days Hands-on time: 5 hr Input quantity: 50 ng DNA Sequencing and microarray kits and reagents help translational and clinical researchers investigate the role of genetic variation in cancer, rare diseases, reproductive health, and more. Our clinical cancer research solutions deliver accurate genomic information, and enable labs to analyze multiple genes in a single test. NGS technology is helping to drive breakthroughs in genetic disease testing by facilitating early detection and diagnosis. As a hypothesis-free method, NGS can distinguish between infectious disease strains that differ by as little as one SNP, and replace multiple tests.