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.
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.
AmpliSeq for Illumina BRCA Panel
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
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
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
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
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
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
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
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
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)
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)
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
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
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
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
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
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
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
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)
This kit is for the extraction, library preparation, and quantitation of cell-free DNA fragments isolated from maternal whole blood samples.
TruSight Cancer
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.