Products for translational and clinical researchers

Helping researchers better understand the role of genetics in disease biology and reproductive health

Clinical Research Products

Areas of Research Focus



Key Use

Cancer Type

Specialized Sample Types

Variant Class
24sure Microarray

Widely used microarray and proven method for accurate, timely preimplantation genetic screening results.

24sure+ Microarray

Microarray to assay whole chromosome copy number imbalances and subchromosomal structural imbalances in polar bodies, blastomeres and blastocysts.

HumanCytoSNP FFPE-12 BeadChip

This BeadChip array is optimized for cytogenetic studies using formalin-fixed paraffin-embedded (FFPE) paired tumor-normal samples.

HumanCytoSNP-12 BeadChip

This 12-sample BeadChip array enables analysis of genetic and structural variation in the human genome, such as duplications, deletions, amplifications, copy-neutral LOH, and mosaicism.

HumanKaryomap-12 DNA Analysis Kit

This genome-wide karyomapping microarray provides insight into the inheritance of single-gene defects by testing single cells from embryo biopsies.

Infinium CytoSNP-850K v1.1 BeadChip

This consortium-built array provides comprehensive coverage of cytogenetically relevant genes for congenital disorders and cancer research.

SureMDA Amplification System

Whole-genome amplification of total DNA from a single embryonic cell, or a few embryonic cells, for use in the karyomapping assay protocol.

SurePlex DNA Amplification System

Used to generate a DNA template from single cells. Ideal for use with 24sure aneuploidy screening arrays or VeriSeq PGS applications.

SureRef Reference DNA

Amplified genomic DNA recommended for use as part of the 24sure protocols when analyzing amplified DNA from a single cell or a few cells.

TruSeq Amplicon - Cancer Panel

The TruSeq Amplicon - Cancer Panel is a highly multiplexed targeted resequencing assay for detecting somatic mutations.

TruSight Cancer

This expert-defined sequencing panel targets 94 genes and 284 SNPs associated with a predisposition towards various cancers.

TruSight Cardio Sequencing Kit

This kit provides researchers with a comprehensive, cost-effective solution for identifying causal variants implicated in inherited cardiac conditions (ICCs).

TruSight HLA v2 Sequencing Panel

Unambiguous, phase-resolved HLA typing in a single assay using proven Illumina NGS technology and Assign analysis software.

TruSight Inherited Disease

TruSight Inherited Disease is a targeted sequencing panel that focuses on 552 genes associated with severe, recessive pediatric onset diseases.

TruSight Myeloid Sequencing Panel

The TruSight Myeloid Sequencing Panel targets variants associated with myeloid malignancies such as AML, MDS, MPN, CML, CMML, and JMML.

TruSight One Sequencing Panel

This panel focuses on exonic regions harboring disease-causing variants. Labs can perform commonly ordered molecular assays on-site with one assay.

TruSight RNA Fusion Panel

Provides comprehensive gene fusion detection in formalin-fixed, paraffin-embedded (FFPE) and other cancer research samples.

TruSight RNA Pan-Cancer

Targeting 1385 cancer genes for gene expression, variant, and fusion detection studies in many RNA sample types including blood, bone marrow, and FFPE.

TruSight Rapid Capture

TruSight Rapid Capture all-in-one kits enable targeted sequencing library preparation and enrichment for up to 96 samples in only 1.5 days.

TruSight Tumor 15

Focused sequencing panel to assess 15 genes that are commonly mutated in solid tumors in a single assay, with a simple, rapid workflow.

TruSight Tumor 170

Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.

TruSight Tumor 26

This targeted sequencing panel enables clinical researchers to identify low-frequency variation in solid tumors across 26 genes.

VeriSeq PGS

A fully validated next-generation sequencing solution for PGS, providing accurate results in aneuploidy screening and extending future opportunities.